NDC 71364-004 Botanic Twenty Daily Sunblock Spf50
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 71364-004?
What are the uses for Botanic Twenty Daily Sunblock Spf50?
Which are Botanic Twenty Daily Sunblock Spf50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Botanic Twenty Daily Sunblock Spf50 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:
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- AMILOXATE (UNII: 376KTP06K8)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CHRYSANTHELLUM INDICUM WHOLE (UNII: YPX537PA31)
- CHAMAECYPARIS OBTUSA LEAF (UNII: 7OL154J5XB)
- STAR ANISE FRUIT (UNII: CK15HA8438)
- STEARYL CAPRYLATE (UNII: 06TS6O9194)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- YELLOW WAX (UNII: 2ZA36H0S2V)
- POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)
- STEARYL HEPTANOATE (UNII: 2M4UGL1NCN)
- NIACINAMIDE (UNII: 25X51I8RD4)
- COPTIS JAPONICA ROOT (UNII: JH0SWT16D1)
- LARIX SIBIRICA WOOD (UNII: KSC3PGF73L)
- LONICERA JAPONICA FLOWER (UNII: 4465L2WS4Y)
- RHEUM PALMATUM ROOT (UNII: G025DAL7CE)
- BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CORYDALIS TURTSCHANINOVII WHOLE (UNII: I94Q8D25FS)
- HOUTTUYNIA CORDATA WHOLE (UNII: O3E12ZLW5T)
- WATER (UNII: 059QF0KO0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
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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".