NDC 47341-002

Burn-B Gone OTC

Burn-b Gone Otc

Burn-B Gone OTC is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Quantum Labs Llc. The primary component is Allantoin.

• Product ID: 47341-002_a6b5ed46-bf0e-4e9e-8ced-a6645ee59148
• NDC: 47341-002
• Product Type: Human Otc Drug
• Proprietary Name: Burn-B Gone OTC
• Generic Name: Burn-b Gone Otc
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-05-10
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part347
• Labeler Name: Quantum Labs LLC
• Substance Name: ALLANTOIN
• Active Ingredient Strength: 1 g/75g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 47341-002-20

75 g in 1 TUBE (47341-002-20)

• Marketing Start Date: 2010-05-10
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 47341-002-20 [47341000220]

Burn-B Gone OTC GEL

• Marketing Category: OTC monograph final
• Application Number: part347
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-10
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ALLANTOIN	.75 g/75g

OpenFDA Data

• SPL SET ID: ace3557b-a08f-4a6e-b911-0bc2fa42141a
• Manufacturer:
  • Quantum Labs LLC
• UNII:
  • 344S277G0Z
• RxNorm Concept Unique ID - RxCUI:
  • 1045330

NDC Crossover Matching brand name "Burn-B Gone OTC" or generic name "Burn-b Gone Otc"

NDC	Brand Name	Generic Name
47341-002	Burn-B Gone OTC	Burn-B Gone OTC
51483-002	Burn-B Gone OTC	Allantoin