NDC 63044-484 Ammonium Lactate
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 63044 - Nnodum Pharmaceuticals
- 63044-484 - Ammonium Lactate
Product Characteristics
Product Packages
NDC Code 63044-484-09
Package Description: 225 g in 1 BOTTLE, PLASTIC
Price per Unit: $0.03299 per GM
Product Details
What is NDC 63044-484?
What are the uses for Ammonium Lactate?
Which are Ammonium Lactate UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMMONIUM LACTATE (UNII: 67M901L9NQ)
- LACTIC ACID (UNII: 33X04XA5AT) (Active Moiety)
Which are Ammonium Lactate 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:
- CETYL ALCOHOL (UNII: 936JST6JCN)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- TROLAMINE (UNII: 9O3K93S3TK)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- WATER (UNII: 059QF0KO0R)
- PETROLATUM (UNII: 4T6H12BN9U)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLENE OXIDE (UNII: Y4Y7NYD4BK)
What is the NDC to RxNorm Crosswalk for Ammonium Lactate?
- RxCUI: 197362 - ammonium lactate 12 % Topical Lotion
- RxCUI: 197362 - ammonium lactate 120 MG/ML Topical Lotion
- RxCUI: 197362 - ammonium lactate 120 MG/ML (as neutralized lactic acid 12 % ) Topical Lotion
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Patient Education
Ammonium Lactate Topical
Ammonium lactate is used to treat xerosis (dry or scaly skin) and ichthyosis vulgaris (an inherited dry skin condition) in adults and children. Ammonium lactate is in a class of medications called alpha-hydroxy acids. It works by increasing skin hydration.
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[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".