NDC 47682-234

Medi-First Sting Relief

Benzocaine 6%, Isopropyl Alcohol 60%

Medi-First Sting Relief is a Topical Swab in the Human Otc Drug category. It is labeled and distributed by Unifirst First Aid Corporation. The primary component is Benzocaine; Isopropyl Alcohol.

• Product ID: 47682-234_6e610821-b031-930b-e053-2a91aa0a66f9
• NDC: 47682-234
• Product Type: Human Otc Drug
• Proprietary Name: Medi-First Sting Relief
• Generic Name: Benzocaine 6%, Isopropyl Alcohol 60%
• Dosage Form: Swab
• Route of Administration: TOPICAL
• Marketing Start Date: 2018-07-02
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part348
• Labeler Name: Unifirst First Aid Corporation
• Substance Name: BENZOCAINE; ISOPROPYL ALCOHOL
• Active Ingredient Strength: 60 mg/mL; mL/mL
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 47682-234-12

10 PACKET in 1 BOX (47682-234-12) > .6 mL in 1 PACKET

• Marketing Start Date: 2018-07-02
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 47682-234-12 [47682023412]

Medi-First Sting Relief SWAB

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-07-02

NDC 47682-234-99 [47682023499]

Medi-First Sting Relief SWAB

• Marketing Category: OTC monograph not final
• Application Number: part348
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-07-02

Drug Details

Active Ingredients

Ingredient	Strength
BENZOCAINE	60 mg/mL

OpenFDA Data

• SPL SET ID: 6e610821-b030-930b-e053-2a91aa0a66f9
• Manufacturer:
  • Unifirst First Aid Corporation
• UNII:
  • ND2M416302
  • U3RSY48JW5
• RxNorm Concept Unique ID - RxCUI:
  • 895749

NDC Crossover Matching brand name "Medi-First Sting Relief" or generic name "Benzocaine 6%, Isopropyl Alcohol 60%"

NDC	Brand Name	Generic Name
47682-234	Medi-First Sting Relief	Benzocaine 6%, Isopropyl alcohol 60%
80514-005	sting relief medicated pad	Benzocaine 6%, Isopropyl alcohol 60%