NDC 75936-503 Lip And Cheek Treat Broad Spectrum Spf 40 Supergoop
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 75936-503?
What are the uses for Lip And Cheek Treat Broad Spectrum Spf 40 Supergoop?
Which are Lip And Cheek Treat Broad Spectrum Spf 40 Supergoop UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Lip And Cheek Treat Broad Spectrum Spf 40 Supergoop 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:
- SHEA BUTTER (UNII: K49155WL9Y)
- HYDROGENATED POLYBUTENE (1300 MW) (UNII: 7D1YQ9Y5EZ)
- SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)
- MICROCRYSTALLINE WAX (UNII: XOF597Q3KY)
- POLYESTER-8 (1400 MW, CYANODIPHENYLPROPENOYL CAPPED) (UNII: T9296U138P)
- CERESIN (UNII: Q1LS2UJO3A)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- CASTOR OIL (UNII: D5340Y2I9G)
- DIISOPROPYL SEBACATE (UNII: J8T3X564IH)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- LAURYL LACTATE (UNII: G5SU0BFK7O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- D&C RED NO. 7 (UNII: ECW0LZ41X8)
- TOCOPHEROL (UNII: R0ZB2556P8)
- SOYBEAN OIL (UNII: 241ATL177A)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- POLYSILICONE-15 (UNII: F8DRP5BB29)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- CRANBERRY (UNII: 0MVO31Q3QS)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- OLIVE OIL (UNII: 6UYK2W1W1E)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- WATER (UNII: 059QF0KO0R)
- CALENDULA OFFICINALIS FLOWER (UNII: P0M7O4Y7YD)
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
* 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".