NDC 80641-002 Vacation Mineral Broad Spectrum Spf 30 Sunscreen
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 80641-002?
What are the uses for Vacation Mineral Broad Spectrum Spf 30 Sunscreen?
Which are Vacation Mineral Broad Spectrum Spf 30 Sunscreen 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 Vacation Mineral 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:
- ALLANTOIN (UNII: 344S277G0Z)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SHEA BUTTER (UNII: K49155WL9Y)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)
- CAPRYLYL GLYCERYL ETHER (UNII: MI97BW74XZ)
- CUCUMBER (UNII: YY7C30VXJT)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- DIHEPTYL SUCCINATE (UNII: 057N7SS26Y)
- GALACTOARABINAN (UNII: SL4SX1O487)
- GLYCERIN (UNII: PDC6A3C0OX)
- HELIANTHUS ANNUUS FLOWERING TOP (UNII: BKJ0J3D1BP)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- METHYL DIHYDROABIETATE (UNII: 7666FJ0J9F)
- NIACIN (UNII: 2679MF687A)
- RICE BRAN (UNII: R60QEP13IC)
- POLYGLYCERYL-2 OLEATE (UNII: 5759J47SAM)
- POLYGLYCERYL-2 STEARATE (UNII: 253MC0P0YV)
- PROPANEDIOL (UNII: 5965N8W85T)
- ROSEMARY (UNII: IJ67X351P9)
- .ALPHA.-TOCOPHEROL (UNII: H4N855PNZ1)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- WATER (UNII: 059QF0KO0R)
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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".