NDC 61995-2437 Al0043700 Alba Botanica Baby Mineral Sunscreen Spf50
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What is NDC 61995-2437?
What are the uses for Al0043700 Alba Botanica Baby Mineral Sunscreen Spf50?
Which are Al0043700 Alba Botanica Baby Mineral Sunscreen Spf50 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 Al0043700 Alba Botanica Baby Mineral Sunscreen 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:
- MICA (UNII: V8A1AW0880)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- ORANGE OIL (UNII: AKN3KSD11B)
- POLYGLYCERYL-3 RICINOLEATE (UNII: MZQ63P0N0W)
- POLYGLYCERYL-2 SESQUIISOSTEARATE (UNII: LA272Q68GQ)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- ALCOHOL (UNII: 3K9958V90M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SHEA BUTTER (UNII: K49155WL9Y)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- JUNIPERUS VIRGINIANA OIL (UNII: PAD4FN7P2G)
- GLYCERYL ISOSTEARATE (UNII: HYE7O27HAO)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- C10-18 TRIGLYCERIDES (UNII: 43AGM4PHPI)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- CHAMOMILE (UNII: FGL3685T2X)
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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".