43857-0284 : Androbalance Oral Spray


NDC: 43857-0284
Labeler: Bioactive Nutritional, Inc.
Product Type: Human OTC Drug
Drug Name: Androbalance
Dosage Form: Oral Spray
Rev. Date: 
CSA Schedule: CIII (US) [1]


[1] Schedule III / IIIN Controlled Substance: Has a potential for abuse less than substances in Schedules I or II and abuse may lead to moderate or low physical dependence or high psychological dependence. (i.e. Products containing not more than 90 milligrams of Codeine per dosage unit [such as Tylenol with Codeine], other narcotics such as Buprenorphine (Suboxone), and Schedule IIIN non-narcotics such as Didrex, Ketamine, Phendimetrazine, and Anabolic Steroids). More Details: US Dept of Justice Controlled Substance Schedules.

NDC Package Codes:

  • 43857-0284-1: 30 ML IN 1 BOTTLE, SPRAY (43857‑0284‑1)

Active Ingredients:

  • Prasterone
  • Pregnenolone
  • Progesterone
  • Testosterone

Dosage Strength:

  • 6 [hp_X]/mL
  • 8 [hp_X]/mL
  • 8 [hp_X]/mL
  • 8 [hp_X]/mL

Pharmaceutical Classes:

  • Androgen Receptor Agonists [MoA]
  • Androgen [EPC]
  • Androstanes [CS]
  • Progesterone [CS]
  • Progesterone [EPC]

Related Products:

Based on records with the same trade name.
  • 43857-0102 Androbalance Oral Liquid by Bioactive Nutritional, Inc.
  • 57520-0023 Androbalance Oral Spray by Apotheca Company

NDC QR Code

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NDC 43857-0284 QR Code

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.