NDC 76485-1025 Rimmel Bb Beauty Balm Medium
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76485-1025?
What are the uses for Rimmel Bb Beauty Balm Medium?
Which are Rimmel Bb Beauty Balm Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Rimmel Bb Beauty Balm Medium 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)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- DOCOSANOL (UNII: 9G1OE216XY)
- ISODECYL NEOPENTANOATE (UNII: W60VYE24XC)
- SHEA BUTTER (UNII: K49155WL9Y)
- METHYL METHACRYLATE (UNII: 196OC77688)
- BEHENETH-25 (UNII: 0G17KJ5M7P)
- GLYCERYL STEARATE SE (UNII: FCZ5MH785I)
- CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L)
- ALUMINUM DIMYRISTATE (UNII: J2KA067N9O)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- EDETATE SODIUM (UNII: MP1J8420LU)
- TOCOPHEROL (UNII: R0ZB2556P8)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
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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".