NDC 82769-100 Everyday Mineral Moisturizer Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 82769-100?
Which are Everyday Mineral Moisturizer Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Everyday Mineral Moisturizer Spf 30 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- ISODODECANE (UNII: A8289P68Y2)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- POLYMETHYLSILSESQUIOXANE/TRIMETHYLSILOXYSILICATE (UNII: X2PZH4Y6HT)
- SQUALANE (UNII: GW89575KF9)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCOYL CAPRYLOCAPRATE (UNII: 8D9H4QU99H)
- POLYGLYCERYL-3 DIISOSTEARATE (UNII: 46P231IQV8)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- TRIHEPTANOIN (UNII: 2P6O7CFW5K)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- TROMETHAMINE (UNII: 023C2WHX2V)
- GLYCERYL MONOCAPRYLATE (UNII: TM2TZD4G4A)
- C18-36 ACID TRIGLYCERIDE (UNII: ZRA72DR3R7)
- DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)
- SUCROSE (UNII: C151H8M554)
- LAUROYL LYSINE (UNII: 113171Q70B)
- PANTHENOL (UNII: WV9CM0O67Z)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- PROPYLENE CARBONATE (UNII: 8D08K3S51E)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- GLYCERYL 1-UNDECYLENATE (UNII: B68LJT9544)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- HYDROXYETHYL CELLULOSE, UNSPECIFIED (UNII: T4V6TWG28D)
- CLOVE (UNII: K48IKT5321)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- RICE GERM (UNII: 7N2B70SFEZ)
- HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)
- SWEET POTATO (UNII: M9WGG9Z9GK)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- BETULA PUBESCENS BARK (UNII: 3R504894L9)
- INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
- REYNOUTRIA JAPONICA LEAF (UNII: 2540B7G25G)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- SACCHAROMYCES LYSATE (UNII: R85W246Z1C)
- CENTELLA ASIATICA WHOLE (UNII: 7M867G6T1U)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
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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".