58593-780 : Finafta Oral Liquid


NDC: 58593-780
Labeler: Efficient Laboratories Inc.
Product Type: Human OTC Drug
Drug Name: Finafta
Dosage Form: Oral Liquid
Application #: part356
Rev. Date: 


NDC Package Codes:

  • 58593-780-15: 15 ML IN 1 BOTTLE, WITH APPLICATOR (58593‑780‑15)

Active Ingredients:

  • Alcohol
  • Benzocaine
  • Salicylic Acid

Dosage Strength:

  • 60 mL/100mL
  • 5 mg/100mL
  • 1 mg/100mL

Pharmaceutical Classes:

  • Allergens [CS]
  • Cell-mediated Immunity [PE]
  • Increased Histamine Release [PE]
  • Standardized Chemical Allergen [EPC]

Related Products:

Based on records with the same trade name.
  • 58593-783 Finafta Topical Liquid by Efficient Laboratories Inc.

NDC QR Code

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NDC 58593-780 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.