NDC 51435-001 Neutracett Ulcer
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51435 - Advanced Biomedics Inc
- 51435-001 - Neutracett
Product Packages
NDC Code 51435-001-01
Package Description: 28.3 g in 1 TUBE
Product Details
What is NDC 51435-001?
What are the uses for Neutracett Ulcer?
Which are Neutracett Ulcer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ALLANTOIN (UNII: 344S277G0Z)
- ALLANTOIN (UNII: 344S277G0Z) (Active Moiety)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Neutracett Ulcer Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- WATER (UNII: 059QF0KO0R)
- HYALURONIC ACID (UNII: S270N0TRQY)
- PANTHENOL (UNII: WV9CM0O67Z)
- PPG-5-CETETH-20 (UNII: 4AAN25P8P4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
What is the NDC to RxNorm Crosswalk for Neutracett Ulcer?
- RxCUI: 1045324 - allantoin 0.5 % / glycerin 5 % Topical Gel
- RxCUI: 1045324 - allantoin 0.005 MG/MG / glycerin 0.05 MG/MG Topical Gel
- RxCUI: 1045328 - Neutracett 0.5 % / 5 % Topical Gel
- RxCUI: 1045328 - allantoin 0.005 MG/MG / glycerin 0.05 MG/MG Topical Gel [Neutracett]
- RxCUI: 1045328 - Neutracett (allantoin 0.5 % / glycerin 5 % ) Topical Gel
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".