NDC 51435-001

NEUTRACETT ULCER

Allantoin Glycerin

NEUTRACETT ULCER is a Topical Gel in the Human Otc Drug category. It is labeled and distributed by Advanced Biomedics Inc. The primary component is Allantoin; Glycerin.

• Product ID: 51435-001_17f26cc3-8018-40e5-a80a-f33323219020
• NDC: 51435-001
• Product Type: Human Otc Drug
• Proprietary Name: NEUTRACETT ULCER
• Generic Name: Allantoin Glycerin
• Dosage Form: Gel
• Route of Administration: TOPICAL
• Marketing Start Date: 2010-05-28
• Marketing Category: OTC MONOGRAPH FINAL / OTC MONOGRAPH FINAL
• Application Number: part347
• Labeler Name: ADVANCED BIOMEDICS INC
• Substance Name: ALLANTOIN; GLYCERIN
• Active Ingredient Strength: 1 mg/.1g; mg/g
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51435-001-01

28.3 g in 1 TUBE (51435-001-01)

• Marketing Start Date: 2010-05-28
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51435-001-01 [51435000101]

NEUTRACETT ULCER GEL

• Marketing Category: OTC monograph final
• Application Number: part347
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2010-05-28
• Inactivation Date: 2019-10-21

Drug Details

Active Ingredients

Ingredient	Strength
ALLANTOIN	.5 mg/.1g

OpenFDA Data

• SPL SET ID: 057335a7-ef93-4b86-8d2f-85fa74f1bd15
• Manufacturer:
  • ADVANCED BIOMEDICS INC
• UNII:
  • 344S277G0Z
  • PDC6A3C0OX
• RxNorm Concept Unique ID - RxCUI:
  • 1045328
  • 1045324

NDC Crossover Matching brand name "NEUTRACETT ULCER" or generic name "Allantoin Glycerin"

NDC	Brand Name	Generic Name
51435-001	NEUTRACETT	ALLANTOIN GLYCERIN
51435-002	NEUTRACETT	ALLANTOIN GLYCERIN
51435-003	NEUTRACETT	ALLANTOIN GLYCERIN