Skip to content

Why is Semaglutide Pink? Unpacking the Role of Compounding

4 min read

As of July 2025, the FDA has received over 600 adverse event reports for compounded semaglutide [1.5.1]. A common question that arises is, 'Why is semaglutide pink?', a trait exclusive to these non-brand versions, often signaling added ingredients [1.2.1, 1.2.2].

Quick Summary

FDA-approved semaglutide like Ozempic is a clear liquid [1.2.2]. A pink or red color indicates a compounded version, most commonly from the addition of vitamin B12 (cyanocobalamin), which is naturally reddish [1.3.1, 1.3.2].

Key Points

  • Not from the Manufacturer: FDA-approved semaglutide (Ozempic, Wegovy) is a clear, colorless liquid; a pink or red color indicates it's a compounded product [1.2.1, 1.2.2].

  • Vitamin B12 is the Cause: The pink hue is most often from the addition of vitamin B12 (cyanocobalamin), which is naturally red in liquid form [1.3.1, 1.3.2].

  • Not FDA-Approved: Compounded drugs, including those mixed with B12, are not reviewed or approved by the FDA for safety, quality, or effectiveness [1.5.1, 1.9.1].

  • Significant Risks: The FDA has issued warnings about compounded semaglutide due to risks of incorrect dosing, contamination, and the use of unapproved active ingredients (salt forms) [1.5.1, 1.5.2, 1.8.4].

  • Claimed Benefits are Unverified: Compounding pharmacies claim adding B12 reduces fatigue and nausea, but these benefits have not been scientifically validated in combination with semaglutide [1.3.4, 1.5.2].

  • Dosing Errors are a Major Concern: Unlike pre-filled brand-name pens, compounded versions often require manual measurement from vials, which has led to serious overdoses [1.5.2].

  • Consult a Professional: Always use medications prescribed by a licensed provider and sourced from a reputable, state-licensed pharmacy to ensure safety [1.7.2].

In This Article

What is Semaglutide?

Semaglutide is a medication belonging to a class of drugs known as glucagon-like peptide-1 (GLP-1) receptor agonists [1.5.2]. It mimics a hormone in the gut that is released after eating, which helps to regulate blood sugar by prompting the body to produce more insulin [1.5.5, 1.6.3]. Beyond its primary function in managing type 2 diabetes, semaglutide also slows down how quickly food leaves the stomach, leading to a feeling of fullness, and it interacts with parts of the brain that control appetite [1.5.5, 1.6.3]. This dual action has made it a highly effective and popular treatment for chronic weight management [1.2.2]. The U.S. Food and Drug Administration (FDA) has approved semaglutide under brand names like Ozempic and Rybelsus for diabetes and Wegovy for weight management [1.5.2, 1.5.6]. These medications are administered either as a once-weekly injection or a daily oral tablet [1.5.2].

The Appearance of FDA-Approved Semaglutide

It is crucial to understand the appearance of official, FDA-approved semaglutide products to have a baseline for comparison. Injectable brand-name medications like Ozempic and Wegovy are manufactured as sterile, clear, and colorless solutions [1.2.2, 1.2.5]. They are supplied in pre-filled pens designed for single-patient use, which have a small window to allow for visual inspection of the liquid before injection [1.2.2]. Any discoloration, cloudiness, or visible particles in an FDA-approved semaglutide pen is a sign of potential contamination or degradation, and the product should not be used [1.2.3, 1.2.5]. Rybelsus, the oral form, is a pale yellow, round tablet [1.2.3]. The official products from the manufacturer are never pink or red [1.2.1].

The Rise of Compounded Semaglutide

Drug compounding is a practice where a licensed pharmacist combines, mixes, or alters ingredients to create a medication tailored to the needs of an individual patient [1.9.2]. This can be necessary for various reasons, such as removing a non-active ingredient that a patient is allergic to or creating a liquid form of a drug for someone who cannot swallow pills [1.7.2]. Due to the massive demand and subsequent shortages of brand-name semaglutide drugs like Wegovy and Ozempic, many patients have turned to compounding pharmacies to access the medication [1.5.3, 1.7.2]. These pharmacies can, in some circumstances like a drug shortage, legally create their own versions of the medication from active pharmaceutical ingredients (APIs) [1.9.4]. However, these compounded versions are not FDA-approved, meaning they do not undergo the same rigorous review for safety, quality, and effectiveness as commercially manufactured drugs [1.5.1, 1.9.1].

So, Why is Semaglutide Pink?

The most common reason for a pink or reddish hue in a vial of semaglutide is that it is a compounded product containing an additional ingredient: Vitamin B12 (cyanocobalamin) [1.2.1, 1.3.1]. Vitamin B12 in its liquid form is naturally red, so when it is mixed with the otherwise clear semaglutide solution, it imparts a pink or red color [1.3.1]. The intensity of the color can vary from light pink to deep red depending on the concentration of B12 added by the compounding pharmacy [1.3.2].

Why Add Vitamin B12?

Compounding pharmacies often market semaglutide with B12 by claiming several benefits. The primary purported advantages include:

  • Mitigating Side Effects: Proponents claim that B12 can help reduce common semaglutide side effects like nausea and gastrointestinal discomfort [1.3.4, 1.6.2].
  • Combating Fatigue: Weight loss and caloric restriction can lead to fatigue. Since B12 is essential for energy metabolism and the production of red blood cells, it is added with the claim that it will boost energy levels [1.3.1, 1.3.5, 1.6.4].
  • Enhanced Metabolism: Some sources suggest that B12 plays a role in fat metabolism, and combining it with semaglutide can enhance the overall weight loss process [1.6.3, 1.6.4].
  • Convenience: Combining the two substances into a single injection is more convenient than administering two separate shots [1.3.1]. It is important to note that the FDA has not evaluated or approved the combination of semaglutide with B12 for safety or effectiveness [1.5.2].

Safety, Regulation, and Risks

The fundamental difference between FDA-approved and compounded semaglutide lies in regulatory oversight. Compounded drugs are not reviewed by the FDA, which raises significant safety concerns [1.7.1, 1.9.1].

FDA Warnings: The FDA has issued numerous warnings regarding compounded semaglutide [1.5.1]. The agency has received hundreds of reports of adverse events, including some requiring hospitalization [1.5.2]. Concerns include:

  • Incorrect Dosing: Compounded drugs often come in multi-dose vials, and confusion over measurements has led to significant overdoses—in some cases, patients have administered up to 20 times the intended dose [1.5.2].
  • Use of Salt Forms: The FDA has found that some compounders are using salt-based forms of semaglutide (e.g., semaglutide sodium, semaglutide acetate) instead of the base form used in approved drugs [1.5.1, 1.8.1]. The agency has not verified the safety or efficacy of these salt forms [1.5.3, 1.8.2].
  • Contamination and Quality: Compounding pharmacies may not adhere to the same sterile manufacturing standards as large pharmaceutical companies, increasing the risk of bacterial contamination or impurities [1.7.3, 1.7.4].
Feature FDA-Approved Semaglutide (e.g., Ozempic, Wegovy) Compounded Semaglutide
Appearance Clear, colorless liquid [1.2.2, 1.2.5] Can be clear, or pink/red if B12 is added [1.2.1]
Regulation FDA-approved for safety, efficacy, and quality [1.5.5] Not FDA-approved; regulated by state pharmacy boards [1.9.1, 1.9.4]
Active Ingredient Semaglutide base [1.8.1] May be semaglutide base or unapproved salt forms [1.8.1]
Packaging Single-use, pre-filled pens with set doses [1.5.2] Often multi-dose vials requiring manual measurement [1.5.2]
Safety Data Extensive clinical trials and post-market surveillance [1.5.5] No rigorous clinical trials for compounded versions [1.3.2, 1.9.5]

Conclusion

If you see semaglutide that is pink, it is a definitive sign that you are dealing with a compounded version, not a brand-name, FDA-approved product like Ozempic or Wegovy [1.2.1, 1.2.2]. The color is typically caused by the addition of vitamin B12 [1.3.1]. While compounding pharmacies propose benefits for this addition, such as reduced fatigue, these formulations lack FDA approval and carry significant risks related to dosing errors, ingredient quality, and contamination [1.5.1, 1.7.1]. Patients should exercise extreme caution and only use medications prescribed by a licensed healthcare provider and obtained from a reputable, state-licensed pharmacy [1.5.1].

For more information on the risks associated with compounded drugs, you can visit the FDA's information page.

Frequently Asked Questions

No. FDA-approved Ozempic and Wegovy are manufactured as a clear, colorless solution. If the medication is colored, it is not the brand-name product [1.2.2, 1.2.5].

Compounding pharmacies claim that adding vitamin B12 helps to boost energy, combat fatigue associated with weight loss, and reduce side effects like nausea [1.3.1, 1.3.4, 1.6.4].

Pink semaglutide is a compounded drug and is not FDA-approved, meaning its safety, quality, and effectiveness have not been verified by the FDA. The agency has warned of risks including dosing errors, contamination, and the use of unapproved ingredients [1.5.1, 1.7.1].

If any semaglutide solution, whether compounded or brand-name, appears cloudy, has changed color unexpectedly, or contains particles, it should not be used. This could indicate contamination or degradation. Contact your pharmacist or healthcare provider immediately [1.2.1, 1.2.3].

Drug compounding by a licensed pharmacist is legal and permissible under certain conditions, such as during a drug shortage or to meet a specific patient's medical need that cannot be met by a commercially available drug [1.7.2, 1.9.4].

FDA-approved drugs like Ozempic use the 'base' form of semaglutide. Some compounding pharmacies have been found using 'salt' forms (e.g., semaglutide acetate), which are different active ingredients that the FDA has not reviewed for safety or efficacy [1.5.1, 1.8.1, 1.8.2].

Because compounded drugs are not FDA-approved, there is no guarantee of their potency or efficacy [1.7.3, 1.9.1]. Inconsistent dosing, different active ingredients, and lack of quality control mean the results can be unpredictable and may carry significant health risks [1.5.2, 1.7.5].

References

  1. 1
  2. 2
  3. 3
  4. 4
  5. 5
  6. 6
  7. 7
  8. 8
  9. 9
  10. 10
  11. 11
  12. 12
  13. 13
  14. 14
  15. 15
  16. 16
  17. 17
  18. 18
  19. 19
  20. 20
  21. 21
  22. 22
  23. 23
  24. 24
  25. 25
  26. 26
  27. 27
  28. 28
  29. 29

Medical Disclaimer

This content is for informational purposes only and should not replace professional medical advice.