NDC 72688-103 Baby Mineral Sunscreen Roll-on Spf-50
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72688 - Project Sunscreen
- 72688-103 - Baby Mineral Sunscreen Roll-on
Product Packages
NDC Code 72688-103-11
Package Description: 85 g in 1 BOTTLE, WITH APPLICATOR
Product Details
What is NDC 72688-103?
What are the uses for Baby Mineral Sunscreen Roll-on Spf-50?
Which are Baby Mineral Sunscreen Roll-on Spf-50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are Baby Mineral Sunscreen Roll-on Spf-50 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)
- BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)
- OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCONUT ALKANES (UNII: 1E5KJY107T)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- STEARYL DIMETHICONE (400 MPA.S AT 50C) (UNII: R327X197HY)
- CETEARYL METHICONE (15000 MW) (UNII: VY9RTR7MSY)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- GALACTOARABINAN (UNII: SL4SX1O487)
- NIACINAMIDE (UNII: 25X51I8RD4)
- CAPRYLOYL GLYCERIN/SEBACIC ACID COPOLYMER (2000 MPA.S) (UNII: N7YC58165T)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PHYSALIS ANGULATA (UNII: W4TKW9D5GG)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PROPANEDIOL (UNII: 5965N8W85T)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
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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".