NDC 58593-780

Finafta

Ethyl Alcohol, Salicylic Acid, Benzocaine

Finafta is a Oral Liquid in the Human Otc Drug category. It is labeled and distributed by Efficient Laboratories Inc.. The primary component is Alcohol; Salicylic Acid; Benzocaine.

• Product ID: 58593-780_000f9877-478d-4b8c-b66f-5ca52b369e0a
• NDC: 58593-780
• Product Type: Human Otc Drug
• Proprietary Name: Finafta
• Generic Name: Ethyl Alcohol, Salicylic Acid, Benzocaine
• Dosage Form: Liquid
• Route of Administration: ORAL
• Marketing Start Date: 1991-10-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part356
• Labeler Name: Efficient Laboratories Inc.
• Substance Name: ALCOHOL; SALICYLIC ACID; BENZOCAINE
• Active Ingredient Strength: 60 mL/100mL; mg/100mL; mg/100mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 58593-780-15

15 mL in 1 BOTTLE, WITH APPLICATOR (58593-780-15)

• Marketing Start Date: 1991-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 58593-780-15 [58593078015]

Finafta LIQUID

• Marketing Category: OTC monograph not final
• Application Number: part356
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 1991-10-01
• Inactivation Date: 2020-01-31
• Reactivation Date: 2020-02-16

Drug Details

Active Ingredients

Ingredient	Strength
ALCOHOL	60 mL/100mL

OpenFDA Data

• SPL SET ID: 1410fa91-d1bc-4797-b888-9b6971f643e0
• Manufacturer:
  • Efficient Laboratories Inc.
• UNII:
  • O414PZ4LPZ
  • U3RSY48JW5
  • 3K9958V90M

NDC Crossover Matching brand name "Finafta" or generic name "Ethyl Alcohol, Salicylic Acid, Benzocaine"

NDC	Brand Name	Generic Name
58593-780	Finafta	Ethyl Alcohol, Salicylic Acid, Benzocaine
58593-781	Finafta	Benzocaine
58593-782	Finafta	Benzocaine