NDC 75936-105 Invincible Setting Powder Spf 45
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What is NDC 75936-105?
What are the uses for Invincible Setting Powder Spf 45?
Which are Invincible Setting Powder Spf 45 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Invincible Setting Powder Spf 45 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- LAUROYL LYSINE (UNII: 113171Q70B)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- WATER (UNII: 059QF0KO0R)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- CETEARETH-25 (UNII: 8FA93U5T67)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- CERAMIDE NP (UNII: 4370DF050B)
- BEHENIC ACID (UNII: H390488X0A)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CERAMIDE NG (UNII: C04977SRJ5)
- CERAMIDE AP (UNII: F1X8L2B00J)
- CERAMIDE 1 (UNII: 5THT33P7X7)
- N-HEXANOYLSPHINGOSINE (UNII: 038753E78J)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".