NDC 6889-0315 Beautipharm Body Moisturizer Spf 10
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 6889-0315?
Which are Beautipharm Body Moisturizer Spf 10 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Beautipharm Body Moisturizer 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)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- DECYL OLEATE (UNII: ZGR06DO97T)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- THEOBROMA GRANDIFLORUM SEED BUTTER (UNII: I711F13FXM)
- FRUCTOSE (UNII: 6YSS42VSEV)
- GLYCERIN (UNII: PDC6A3C0OX)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- STEARETH-7 (UNII: 820H8P0BYX)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CARBOMER HOMOPOLYMER TYPE C (UNII: 4Q93RCW27E)
- OPUNTIA FICUS-INDICA FLOWER (UNII: 83YSP51SMA)
- LEVOMENOL (UNII: 24WE03BX2T)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- BILBERRY (UNII: 9P2U39H18W)
- DEHYDROACETIC ACID (UNII: 2KAG279R6R)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- 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".