NDC 67938-2076 Pro Triple Protection Factor Face And Body Broad Spectrum Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 67938-2076?
What are the uses for Pro Triple Protection Factor Face And Body Broad Spectrum Spf 30 Sunscreen?
Which are Pro Triple Protection Factor Face And Body Broad Spectrum Spf 30 Sunscreen UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Pro Triple Protection Factor Face And Body Broad Spectrum Spf 30 Sunscreen 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)
- NYLON-12 (UNII: 446U8J075B)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)
- CETETH-20 PHOSPHATE (UNII: 921FTA1500)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- COCO GLUCOSIDE (UNII: ICS790225B)
- CARNOSINE (UNII: 8HO6PVN24W)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- ACETYL FARNESYLCYSTEINE (UNII: KK6984C8O3)
- EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)
- CHONDRUS CRISPUS CARRAGEENAN (UNII: UE856F2T78)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- ARABIDOPSIS THALIANA (UNII: AI3L60HQ81)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
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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".