NDC 82063-6598 Unisex Bb Tint- It S Clear - 6598
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What is NDC 82063-6598?
What are the uses for Unisex Bb Tint- It S Clear - 6598?
Which are Unisex Bb Tint- It S Clear - 6598 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Unisex Bb Tint- It S Clear - 6598 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)
- COCO-CAPRYLATE (UNII: 4828G836N6)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- SHEA BUTTER ETHYL ESTERS (UNII: V2CI786FPG)
- C15-19 ALKANE (UNII: CI87N1IM01)
- GLYCERIN (UNII: PDC6A3C0OX)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POLYGLYCERYL-6 POLYRICINOLEATE (UNII: YPM0ZOC2HR)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- AVOCADO OIL (UNII: 6VNO72PFC1)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- ASIAN GINSENG (UNII: CUQ3A77YXI)
- CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
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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".