68071-4589 : Biofreeze Professional 50 mg/ml Topical Gel


NDC: 68071-4589
Labeler: Nucare Pharmaceuticals, Inc.
Product Type: Human OTC Drug
Drug Name: Biofreeze Professional
Dosage Form: Topical Gel
Application #: part348
Rev. Date: 


NDC Package Codes:

  • 68071-4589-4: 118 ML IN 1 TUBE (68071‑4589‑4)

Active Ingredients:

  • Menthol
  • Unspecified Form

Dosage Strength:

  • 50 mg/mL

Related Products:

Based on records with the same trade name.
  • 68071-4325 Biofreeze Professional 50 mg/ml Topical Gel by Nucare Pharmaceuticals, Inc.
  • 50090-6367 Biofreeze Professional 50 mg/ml Topical Gel by A-s Medication Solutions
  • 59316-115 Biofreeze Professional 50 mg/ml Topical Gel by Performance Health, LLC
  • 59316-119 Biofreeze Professional 50 mg/ml Topical Gel by Performance Health, LLC
  • 59316-120 Biofreeze Professional 105 mg/ml Topical Spray by Performance Health, LLC
  • 59316-834 Biofreeze Professional 105 mg/ml Topical Aerosol, Spray by Rb Health (Us) LLC

NDC 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.