NDC 11489-061 No7 Advanced Hydration Day Sunscreen Spf 12
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What is NDC 11489-061?
What are the uses for No7 Advanced Hydration Day Sunscreen Spf 12?
Which are No7 Advanced Hydration Day Sunscreen Spf 12 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are No7 Advanced Hydration Day Sunscreen Spf 12 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- LIGHT MINERAL OIL (UNII: N6K5787QVP)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- PANTHENOL (UNII: WV9CM0O67Z)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
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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".