NDC 70884-101 Tropicsurf Extreme Protection Spf30-ultra
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What is NDC 70884-101?
What are the uses for Tropicsurf Extreme Protection Spf30-ultra?
Which are Tropicsurf Extreme Protection Spf30-ultra 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 Tropicsurf Extreme Protection Spf30-ultra 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARETH-2 (UNII: V56DFE46J5)
- VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)
- STEARETH-21 (UNII: 53J3F32P58)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- PLUM (UNII: 67M3EQ6BE1)
- PODOCARPUS ELATUS WHOLE (UNII: H38807Y47G)
- KAKADU PLUM (UNII: 0ZQ1D2FDLI)
- ADANSONIA DIGITATA SEED OIL (UNII: 77MKL7AR5I)
- ASTROCARYUM ACULEATUM SEED OIL (UNII: JUP28JPX3K)
- MACADAMIA OIL (UNII: 515610SU8C)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PROPANEDIOL (UNII: 5965N8W85T)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- ALCOHOL (UNII: 3K9958V90M)
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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".