NDC 64760-208 Glytone Retexturize Body
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 64760-208?
What are the uses for Glytone Retexturize Body?
Which are Glytone Retexturize Body UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Glytone Retexturize Body 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)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- GLYCERIN (UNII: PDC6A3C0OX)
- AMMONIA (UNII: 5138Q19F1X)
- POLYETHYLENE GLYCOL 6000 (UNII: 30IQX730WE)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- SHEA BUTTER (UNII: K49155WL9Y)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)
- LAURETH-7 (UNII: Z95S6G8201)
* 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".