NDC 6889-0312 Beautipharm All Day Moisturizing Balm Spf 10
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 6889-0312?
Which are Beautipharm All Day Moisturizing Balm Spf 10 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Beautipharm All Day Moisturizing Balm Spf 10 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DECYL OLEATE (UNII: ZGR06DO97T)
- COCOA BUTTER (UNII: 512OYT1CRR)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CARBOMER COPOLYMER TYPE B (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 809Y72KV36)
- .ALPHA.-BISABOLOL, (+)- (UNII: 105S6I733Z)
- OPUNTIA FICUS-INDICA FLOWER (UNII: 83YSP51SMA)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- BILBERRY (UNII: 9P2U39H18W)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- SUGARCANE (UNII: 81H2R5AOH3)
- ALLANTOIN (UNII: 344S277G0Z)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON (UNII: 24RS0A988O)
- LACTIC ACID (UNII: 33X04XA5AT)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ACER SACCHARUM BARK/SAP (UNII: Z120VL0KAC)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
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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".