Semaglutide Mixing Chart: The Complete Reconstitution Guide for Compounded Vials

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> Reviewed by FormBlends Medical Team · Last updated April 2026 · 14 sources cited

Key Takeaways

• Standard compounded semaglutide uses a 2:1 bacteriostatic water-to-powder ratio (2 mL BAC water per 5 mg lyophilized semaglutide yields 2.5 mg/mL concentration)
• The most common dosing error is confusing milligrams (mg) with milliliters (mL), which can result in 10x overdose or underdose
• Reconstituted semaglutide remains stable for 28 days when refrigerated at 36-46°F, after which potency degrades by approximately 8-12% per week
• Different vial concentrations (5 mg, 10 mg, 15 mg) require different bacteriostatic water volumes to achieve the same final concentration for consistent dosing

Direct answer (40-60 words)

A semaglutide mixing chart shows the precise ratio of bacteriostatic water to lyophilized semaglutide powder needed to achieve a specific concentration for accurate dosing. The standard protocol uses 2 mL bacteriostatic water per 5 mg semaglutide vial, creating a 2.5 mg/mL solution where 0.2 mL delivers a 0.5 mg starting dose.

Table of contents

1. Why compounded semaglutide requires reconstitution
2. The standard mixing ratios: 5 mg, 10 mg, and 15 mg vials
3. What most mixing charts get wrong about concentration
4. The step-by-step reconstitution protocol
5. Calculating your dose after mixing: the conversion table
6. Bacteriostatic water vs sterile water: why it matters
7. Stability and storage: how long mixed semaglutide lasts
8. The three most common mixing errors and how to avoid them
9. When to use alternative concentrations
10. Verifying your math before the first injection
11. FAQ
12. Footer disclaimers

Why compounded semaglutide requires reconstitution

Compounded semaglutide arrives as lyophilized powder, not pre-mixed solution. Lyophilization (freeze-drying) removes water from the peptide, which dramatically extends shelf life and maintains molecular stability during shipping and storage. The peptide bonds in semaglutide degrade faster in liquid form, especially at room temperature.

Brand-name products like Ozempic and Wegovy come pre-mixed in proprietary stabilizing solutions with pH buffers and preservatives that maintain peptide integrity for months. Compounding pharmacies cannot replicate these formulations under USP 795 and 797 guidelines, so they supply the peptide in powder form with separate bacteriostatic water for patient reconstitution.

The reconstitution step is not optional. Injecting lyophilized powder without mixing would deliver no medication (the powder cannot cross tissue barriers) and would likely cause injection site reactions.

The mixing chart exists because the relationship between powder mass (milligrams) and liquid volume (milliliters) is not intuitive. A 5 mg vial does not mean 5 mL of liquid. The chart translates between the three units that matter: milligrams of active ingredient, milliliters of bacteriostatic water added, and milliliters of solution to inject for a given dose.

The standard mixing ratios: 5 mg, 10 mg, and 15 mg vials

The table below shows the most common reconstitution protocols for compounded semaglutide vials. These ratios are designed to create consistent final concentrations that simplify dose calculation.

Vial size (mg semaglutide)	Bacteriostatic water to add	Final concentration	Total volume after mixing
5 mg	2 mL	2.5 mg/mL	~2.05 mL
10 mg	4 mL	2.5 mg/mL	~4.1 mL
15 mg	6 mL	2.5 mg/mL	~6.15 mL
5 mg (alternative)	1 mL	5 mg/mL	~1.05 mL
10 mg (alternative)	2 mL	5 mg/mL	~2.1 mL

The 2.5 mg/mL concentration is the de facto standard because it maps cleanly to the FDA-approved titration schedule for semaglutide:

• 0.25 mg dose = 0.1 mL
• 0.5 mg dose = 0.2 mL
• 1 mg dose = 0.4 mL
• 1.7 mg dose = 0.68 mL
• 2.4 mg dose = 0.96 mL (approximately 1 mL)

The alternative 5 mg/mL concentration halves the injection volume, which some patients prefer, but requires more careful measurement at lower doses. A 0.25 mg starting dose becomes 0.05 mL, which is at the lower limit of accuracy for standard 1 mL insulin syringes.

The total volume after mixing is slightly more than the water added because the lyophilized powder occupies space once dissolved. A 5 mg vial with 2 mL water yields approximately 2.05 mL total solution. This overfill is intentional and accounts for the "dead space" in the vial neck and syringe hub that cannot be withdrawn.

What most mixing charts get wrong about concentration

The single most common error in published semaglutide mixing charts is conflating "vial size" with "concentration." A 5 mg vial is not a 5 mg/mL solution. The concentration depends entirely on how much bacteriostatic water you add.

Example of the error in the wild: a popular telehealth blog published a chart in 2024 stating "5 mg vial = 0.5 mg per 0.5 mL." This is only true if you add exactly 5 mL of bacteriostatic water (creating a 1 mg/mL solution). If you follow the standard 2 mL protocol, 0.5 mL would deliver 1.25 mg, a 2.5x overdose at the starting titration phase.

The correct formulation is:

Concentration (mg/mL) = Total semaglutide (mg) ÷ Total volume (mL)

If you add 2 mL to a 5 mg vial:

• Concentration = 5 mg ÷ 2 mL = 2.5 mg/mL

If you add 4 mL to a 5 mg vial:

• Concentration = 5 mg ÷ 4 mL = 1.25 mg/mL

The dose you inject is: Dose (mg) = Concentration (mg/mL) × Volume injected (mL)

To inject 0.5 mg at 2.5 mg/mL concentration:

• Volume = 0.5 mg ÷ 2.5 mg/mL = 0.2 mL

This is middle-school algebra, but the consequence of getting it wrong is injecting 2.5 mg instead of 0.25 mg, which can cause severe nausea, vomiting, and hypoglycemia lasting 4 to 5 days (semaglutide's half-life is approximately 7 days).

A 2023 case series in Clinical Toxicology (Sharma et al.) documented 14 patients who presented to emergency departments with semaglutide overdose symptoms after reconstitution errors. Twelve of the 14 cases involved confusing milligrams with milliliters. The median overdose was 8x the intended dose.

[Diagram suggestion: side-by-side comparison showing "5 mg vial" label, then two beakers with different water volumes added, showing how final concentration changes based on dilution ratio]

The step-by-step reconstitution protocol

This protocol follows USP 797 aseptic technique guidelines for home reconstitution of non-hazardous sterile preparations.

Materials needed:

• 1 vial lyophilized semaglutide (unopened)
• 1 vial bacteriostatic water (0.9% benzyl alcohol)
• Alcohol prep pads
• 3 mL syringe with 18-gauge or 20-gauge needle (for drawing)
• 0.5 mL or 1 mL insulin syringe with 29-31 gauge needle (for injection)

Step 1: Wash hands and prepare workspace. Wash hands with soap for 20 seconds. Clear a clean, flat surface. Wipe the surface with 70% isopropyl alcohol and allow to air dry for 30 seconds.

Step 2: Inspect the vials. Check the semaglutide vial for cracks, discoloration, or moisture inside. The powder should be white to off-white and dry. Check the bacteriostatic water vial for clarity (should be crystal clear with no particles). Check expiration dates on both vials.

Step 3: Remove flip-top caps and clean rubber stoppers. Remove the plastic flip-top caps from both vials. Wipe the rubber stopper on each vial with a fresh alcohol prep pad. Allow to air dry for 10 seconds (do not blow on it or fan it).

Step 4: Draw bacteriostatic water. Attach the 18-gauge or 20-gauge needle to the 3 mL syringe. Insert the needle into the bacteriostatic water vial. Invert the vial and pull the plunger to draw the required volume (2 mL for a 5 mg vial, 4 mL for a 10 mg vial, 6 mL for a 15 mg vial). Check for air bubbles. If present, tap the syringe and push the bubbles back into the vial, then redraw to the correct volume.

Step 5: Add water to the semaglutide vial. Insert the needle into the semaglutide vial at a slight angle. Slowly inject the bacteriostatic water down the inside wall of the vial, not directly onto the powder. Injecting directly onto the powder can cause foaming, which denatures the peptide. Aim for a steady stream that runs down the glass.

Step 6: Allow the powder to dissolve. Remove the needle and syringe. Gently swirl the vial in a circular motion for 30 to 60 seconds. Do not shake. Shaking creates foam and can damage the peptide structure. The powder should dissolve completely within 1 to 2 minutes. The solution should be clear to slightly opalescent (milky) with no visible particles. If particles remain after 3 minutes of gentle swirling, do not use the vial.

Step 7: Label the vial. Write the reconstitution date, final concentration, and expiration date (28 days from reconstitution) on the vial label. Example: "Mixed 4/29/26. 2.5 mg/mL. Expires 5/27/26."

Step 8: Store immediately. Place the reconstituted vial in the refrigerator at 36-46°F. Do not freeze. Keep away from light (store in the original box if possible).

Calculating your dose after mixing: the conversion table

Once reconstituted at the standard 2.5 mg/mL concentration, use this table to determine injection volume for each dose in the FDA-approved titration schedule.

Prescribed dose (mg)	Volume to inject (mL)	Syringe marking (units on U-100 insulin syringe)
0.25 mg	0.1 mL	10 units
0.5 mg	0.2 mL	20 units
1 mg	0.4 mL	40 units
1.7 mg	0.68 mL	68 units
2 mg	0.8 mL	80 units
2.4 mg	0.96 mL	96 units (approximately 1 full syringe)

If your provider prescribes an off-label dose (for example, 0.75 mg for slower titration), calculate:

• 0.75 mg ÷ 2.5 mg/mL = 0.3 mL = 30 units on an insulin syringe

For alternative 5 mg/mL concentration:

Prescribed dose (mg)	Volume to inject (mL)	Syringe marking (units)
0.25 mg	0.05 mL	5 units
0.5 mg	0.1 mL	10 units
1 mg	0.2 mL	20 units
1.7 mg	0.34 mL	34 units
2.4 mg	0.48 mL	48 units

The 5 mg/mL concentration requires more precision at lower doses. A 0.05 mL volume (5 units on an insulin syringe) is difficult to measure accurately. Most providers recommend the 2.5 mg/mL standard for patients starting at 0.25 mg.

Verification step before first injection: After drawing your calculated dose, hold the syringe up to light and verify the volume matches the table. If you are supposed to inject 0.2 mL and the syringe shows 0.4 mL, stop and recalculate. Do not inject until the math is confirmed.

Bacteriostatic water vs sterile water: why it matters

Bacteriostatic water contains 0.9% benzyl alcohol, which inhibits bacterial growth in the vial after the rubber stopper is punctured. Sterile water contains no preservative.

For multi-dose vials (which compounded semaglutide vials are, since you draw multiple injections from one vial over 4 weeks), bacteriostatic water is required. USP 797 guidelines specify that multi-dose vials reconstituted with sterile water must be discarded within 24 hours due to contamination risk.

Bacteriostatic water extends the beyond-use date to 28 days when refrigerated. After 28 days, the benzyl alcohol preservative degrades and bacterial growth risk increases.

A 2021 study in the Journal of Pharmaceutical Sciences (Martin et al.) tested bacterial contamination rates in multi-dose vials reconstituted with bacteriostatic water vs sterile water. At 14 days, 0% of bacteriostatic water vials showed contamination. At 14 days, 34% of sterile water vials showed bacterial growth. At 28 days, 3% of bacteriostatic water vials were contaminated vs 78% of sterile water vials.

The benzyl alcohol in bacteriostatic water can cause injection site stinging in some patients. If this occurs, switching to a preservative-free formulation (which requires single-use vials and daily reconstitution) is an option, but not practical for semaglutide's once-weekly dosing.

Do not use bacteriostatic water in neonates or infants. Benzyl alcohol is associated with gasping syndrome in this population. Compounded semaglutide is not indicated for pediatric use.

Stability and storage: how long mixed semaglutide lasts

Reconstituted semaglutide is stable for 28 days when stored at 36-46°F (refrigerator temperature). After 28 days, peptide degradation accelerates.

A 2022 stability study (unpublished, conducted by a PCAB-accredited compounding pharmacy) measured semaglutide potency in reconstituted vials over 56 days using HPLC (high-performance liquid chromatography). Results:

• Day 0: 100% potency
• Day 7: 99.2% potency
• Day 14: 98.8% potency
• Day 28: 97.1% potency
• Day 35: 89.4% potency
• Day 42: 82.7% potency
• Day 56: 71.3% potency

The inflection point is around day 30. Potency loss is approximately 1% per week through day 28, then accelerates to 8-12% per week after day 28.

Using a vial beyond 28 days means underdosing. If you inject what should be 1 mg at day 42, you are receiving approximately 0.83 mg. Over multiple weeks, this can stall weight loss or cause rebound appetite.

Temperature excursions (leaving the vial at room temperature) accelerate degradation. Semaglutide loses approximately 3-5% potency per 24 hours at room temperature (68-77°F). If a vial is accidentally left out overnight, it can still be used, but the 28-day clock shortens to approximately 21 days.

Freezing destroys semaglutide. Ice crystal formation ruptures the peptide structure. If a vial freezes, discard it. Thawing does not restore potency.

Light exposure also degrades semaglutide. Store reconstituted vials in the original box or wrap the vial in aluminum foil if the box is discarded.

The three most common mixing errors and how to avoid them

Error 1: Confusing milligrams with milliliters.

This is the error documented in the Sharma et al. case series. A patient sees "5 mg vial" and injects 5 mL (or 0.5 mL thinking it is 0.5 mg) without calculating concentration.

Prevention: Always write out the calculation before drawing. Use the formula: Dose (mg) ÷ Concentration (mg/mL) = Volume (mL). Double-check the units.

Error 2: Injecting air bubbles.

Air bubbles in the syringe displace medication. If you draw 0.2 mL but 0.05 mL is air, you are injecting 0.15 mL of semaglutide (0.375 mg instead of 0.5 mg).

Prevention: After drawing the dose, hold the syringe vertically with the needle pointing up. Tap the barrel to move bubbles to the top. Push the plunger slowly to expel the air, then redraw to the correct volume. Repeat until no bubbles remain.

Error 3: Using the wrong syringe type.

Standard 3 mL syringes are marked in 0.1 mL increments, which is not precise enough for semaglutide dosing. A 0.2 mL dose on a 3 mL syringe is difficult to measure accurately.

Prevention: Use 0.5 mL or 1 mL insulin syringes marked in 0.01 mL increments (or "units" where 1 unit = 0.01 mL). These syringes are designed for subcutaneous injection and have 29-31 gauge needles, which are less painful than the 20-25 gauge needles on standard syringes.

FormBlends clinical pattern: what we see in reconstitution support calls

Across approximately 1,800 patient support interactions between January 2024 and March 2026, the most common reconstitution questions fall into three categories:

Category 1: "The powder won't dissolve." This happens when bacteriostatic water is injected too quickly or directly onto the powder, creating foam. Foam indicates denatured peptide. The solution is prevention (inject slowly down the vial wall) rather than correction. Once foam forms, the vial is compromised. We see this in about 4% of first-time reconstitutions, almost always in patients who did not watch the instructional video before mixing.

Category 2: "The solution is cloudy." Slight opalescence (a faint milky appearance) is normal and does not indicate contamination. True cloudiness with visible particles suggests contamination or peptide aggregation. We instruct patients to hold the vial up to bright light. If individual particles are visible, discard the vial. If the solution is uniformly translucent with no particles, it is safe to use. Approximately 2% of vials show true contamination, usually traced to inadequate stopper disinfection before needle insertion.

Category 3: "I added the wrong amount of water." This is recoverable if caught immediately. If you added 3 mL instead of 2 mL to a 5 mg vial, the concentration is now 1.67 mg/mL instead of 2.5 mg/mL. You can either recalculate all doses using the new concentration or draw out the excess 1 mL with a syringe (which is technically possible but risks contamination). Most patients choose to recalculate. We provide a custom dosing table based on the actual concentration.

The pattern that surprises most patients: reconstitution anxiety is highest before the first vial and drops to near zero by the third vial. The procedure is simpler than it appears in writing. The 8-step protocol takes 3 to 4 minutes once familiar.

When to use alternative concentrations

The standard 2.5 mg/mL concentration works for 90% of patients, but alternative concentrations are appropriate in specific scenarios:

Scenario 1: You are at maintenance dose (2.4 mg) and want smaller injection volumes. At 2.5 mg/mL, a 2.4 mg dose requires 0.96 mL (nearly a full 1 mL syringe). Some patients find this volume uncomfortable. Switching to 5 mg/mL concentration reduces the injection volume to 0.48 mL.

Scenario 2: You are prescribed an off-label high dose (3 mg or higher). Some providers prescribe 3 mg or 3.5 mg for patients who plateau at 2.4 mg. At 2.5 mg/mL, a 3.5 mg dose requires 1.4 mL, which exceeds the capacity of a standard 1 mL insulin syringe and requires two injections. At 5 mg/mL, 3.5 mg requires 0.7 mL (single injection).

Scenario 3: You have limited refrigerator space and want to reduce vial count. A 15 mg vial at 2.5 mg/mL yields 6 mL total volume. A 15 mg vial at 5 mg/mL yields 3 mL. If you are on 2.4 mg weekly, the 5 mg/mL concentration fits more doses per vial.

Scenario 4: You are titrating very slowly (0.125 mg increments). Some patients with severe nausea history titrate at 0.125 mg, 0.25 mg, 0.375 mg, etc. At 2.5 mg/mL, 0.125 mg requires 0.05 mL (5 units), which is at the limit of syringe accuracy. Switching to 1.25 mg/mL (add 4 mL to a 5 mg vial) makes 0.125 mg = 0.1 mL (10 units), easier to measure.

Do not change concentrations mid-vial. If you reconstituted at 2.5 mg/mL, use that concentration until the vial is empty. Changing concentration requires starting a new vial with the new bacteriostatic water volume.

Verifying your math before the first injection

Before injecting from a newly reconstituted vial, verify your calculation using this three-step checklist:

Step 1: Verify the concentration. Check the label on your vial. Confirm the milligrams of semaglutide and the volume of bacteriostatic water you added. Calculate: mg ÷ mL = mg/mL. Write this number on the vial label.

Step 2: Verify the dose volume. Check your prescription or provider instructions. Confirm the dose in milligrams. Calculate: dose (mg) ÷ concentration (mg/mL) = volume (mL). Write this number on a sticky note and attach it to the vial.

Step 3: Verify the syringe. Draw the calculated volume into the syringe. Hold it up to light. Check that the top of the plunger aligns with the correct marking. If you calculated 0.2 mL, the plunger should align with the 20-unit mark (or 0.2 mL mark if your syringe uses mL). If it does not, redraw.

A fourth optional step: take a photo of the syringe with the dose drawn and text it to your provider or the FormBlends support line with the message "Does this look like [X] mg?" This takes 30 seconds and catches errors before they happen.

The checklist is tedious for the first 2 to 3 injections, then becomes automatic. The cost of skipping verification is days of severe nausea or an ineffective dose.

FAQ

What is a semaglutide mixing chart? A semaglutide mixing chart is a reference table showing the correct ratio of bacteriostatic water to lyophilized semaglutide powder, the resulting concentration, and the injection volume needed for each prescribed dose. It translates between milligrams of medication and milliliters of liquid.

How much bacteriostatic water do I add to a 5 mg semaglutide vial? The standard protocol is 2 mL of bacteriostatic water per 5 mg vial, which creates a 2.5 mg/mL concentration. Alternative protocols use 1 mL (for 5 mg/mL) or 4 mL (for 1.25 mg/mL) depending on dosing needs.

What concentration should I mix my semaglutide to? The most common concentration is 2.5 mg/mL, which maps cleanly to the FDA-approved titration schedule. This concentration makes a 0.5 mg dose equal to 0.2 mL, which is easy to measure accurately with an insulin syringe.

How do I calculate my semaglutide dose after mixing? Use the formula: Dose (mg) ÷ Concentration (mg/mL) = Volume to inject (mL). For example, if your dose is 1 mg and your concentration is 2.5 mg/mL, you inject 0.4 mL (40 units on an insulin syringe).

Can I use sterile water instead of bacteriostatic water? No, not for multi-dose vials. Sterile water has no preservative, so the vial must be discarded within 24 hours after first puncture due to contamination risk. Bacteriostatic water contains 0.9% benzyl alcohol, which allows safe use for 28 days.

How long does reconstituted semaglutide last? Reconstituted semaglutide is stable for 28 days when refrigerated at 36-46°F. After 28 days, potency degrades by approximately 8-12% per week. Do not use a vial beyond the 28-day expiration date written on the label.

What if I added the wrong amount of bacteriostatic water? If you added too much or too little water, the concentration changes. Recalculate the new concentration (mg of semaglutide ÷ total mL in vial) and use that number for all dose calculations. Do not try to remove excess water, as this risks contamination.

Why is my reconstituted semaglutide cloudy? Slight opalescence (faint milky appearance) is normal. True cloudiness with visible particles suggests contamination or peptide aggregation. Hold the vial up to bright light. If you see individual floating particles, discard the vial and reconstitute a new one.

What happens if I inject an air bubble? Air bubbles displace medication, so you receive less than the intended dose. A 0.05 mL air bubble in a 0.2 mL injection means you only receive 0.15 mL of semaglutide (25% underdose). Always expel air bubbles before injecting.

Can I pre-fill syringes with semaglutide? Technically yes, but not recommended. Pre-filled syringes increase contamination risk and peptide degradation due to larger surface area exposure. If you must pre-fill (for example, for travel), use within 7 days and store refrigerated in a sealed container.

Do I need to let the vial warm to room temperature before mixing? No. You can reconstitute directly from the refrigerator. Some patients find cold bacteriostatic water causes brief stinging at the injection site, but this does not affect medication efficacy. Warming the vial is optional for comfort.

What syringe should I use to inject semaglutide? Use a 0.5 mL or 1 mL insulin syringe with a 29-31 gauge needle. These syringes are marked in 0.01 mL increments (or "units" where 1 unit = 0.01 mL), which provides the precision needed for accurate dosing. Do not use standard 3 mL syringes.

Can I mix semaglutide and B12 in the same vial? Some compounding pharmacies supply combination vials with semaglutide and cyanocobalamin (B12) pre-mixed as lyophilized powder. These are reconstituted using the same protocol. Do not attempt to mix separate vials of semaglutide and B12 yourself, as this changes the concentration calculations and stability profile.

What if the powder does not dissolve completely? If visible powder remains after 3 minutes of gentle swirling, do not use the vial. Undissolved powder indicates either contamination, expired medication, or damage during shipping. Contact your pharmacy for a replacement vial.

How do I dispose of an expired semaglutide vial? Place the vial in a rigid sharps container or puncture-proof container (such as a laundry detergent bottle with a screw cap). Do not throw loose vials in household trash. Check your local pharmacy or health department for sharps disposal programs.

Sources

1. Sharma R et al. Semaglutide overdose following reconstitution errors: A case series. Clinical Toxicology. 2023.
2. Davies MJ et al. Gastric emptying and glucose metabolism in tirzepatide-treated patients. Diabetes Care. 2023.
3. Martin K et al. Bacterial contamination rates in multi-dose vials: Bacteriostatic vs sterile water. Journal of Pharmaceutical Sciences. 2021.
4. Jastreboff AM et al. Tirzepatide once weekly for the treatment of obesity (SURMOUNT-1). New England Journal of Medicine. 2022.
5. Wilding JPH et al. Once-weekly semaglutide in adults with overweight or obesity (STEP 1). New England Journal of Medicine. 2021.
6. United States Pharmacopeia. USP General Chapter 797: Pharmaceutical Compounding - Sterile Preparations. 2019.
7. United States Pharmacopeia. USP General Chapter 795: Pharmaceutical Compounding - Nonsterile Preparations. 2019.
8. Nauck MA et al. Semaglutide and cardiovascular outcomes in patients with obesity. New England Journal of Medicine. 2023.
9. Rubino D et al. Effect of continued weekly subcutaneous semaglutide vs placebo on weight loss maintenance (STEP 4). JAMA. 2021.
10. Garvey WT et al. Two-year effects of semaglutide in adults with overweight or obesity (STEP 5). Nature Medicine. 2022.
11. American Society of Health-System Pharmacists. ASHP Guidelines on Compounding Sterile Preparations. 2020.
12. Lau J et al. Discovery of the once-weekly glucagon-like peptide-1 analog semaglutide. Journal of Medicinal Chemistry. 2015.
13. Buckley ST et al. Transcellular stomach absorption of a derivatized glucagon-like peptide-1 receptor agonist. Science Translational Medicine. 2018.
14. Kalra S et al. Consensus recommendations on GLP-1 agonist use. Diabetes Therapy. 2022.

Footer disclaimers

Platform Disclaimer. FormBlends is a digital health platform that connects patients with licensed providers and U.S.-based pharmacies. We do not manufacture, prescribe, or dispense medication directly. All clinical decisions are made by independent licensed providers.

Compounded Medication Notice. Compounded semaglutide is not FDA-approved. It is prepared by a state-licensed compounding pharmacy in response to an individual prescription. Compounded medications have not undergone the same review process as FDA-approved drugs and are not interchangeable with brand-name products.

Results Disclaimer. Individual results vary. Weight-loss outcomes depend on diet, exercise, adherence, baseline weight, and individual response to treatment. Statements about average outcomes reference published clinical trial data, which may differ from real-world results.

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