NDC 43596-0885 Ultra Balm Moisturizing Protective Balm For Lips Spf 20 Nude Translucide
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43596 - Ventura Corporation Ltd
- 43596-0885 - Ultra Balm Moisturizing Protective Balm For Lips Spf 20 Nude Translucide
Product Packages
NDC Code 43596-0885-1
Package Description: 4 g in 1 CARTON
Product Details
What is NDC 43596-0885?
What are the uses for Ultra Balm Moisturizing Protective Balm For Lips Spf 20 Nude Translucide?
Which are Ultra Balm Moisturizing Protective Balm For Lips Spf 20 Nude Translucide UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Ultra Balm Moisturizing Protective Balm For Lips Spf 20 Nude Translucide 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:
- BRAZILIAN PEPPER (UNII: SUG822G7CD)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- NEOPENTYL GLYCOL DICAPRYLATE/DICAPRATE (UNII: VLW429K27K)
- OCTYLDODECANOL (UNII: 461N1O614Y)
- CARNAUBA WAX (UNII: R12CBM0EIZ)
- CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- HELIANTHUS ANNUUS SEED WAX (UNII: 42DG15CHXV)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ACACIA DECURRENS FLOWER WAX (UNII: AU6XZE9IY9)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- DIPENTAERYTHRITYL HEXACAPRYLATE/HEXACAPRATE (UNII: 554N82UWVW)
- TRIDECYL TRIMELLITATE (UNII: FY36J270ES)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- CERESIN (UNII: Q1LS2UJO3A)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIDECYL STEARATE (UNII: A8OE252M6L)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN)
- CERAMIDE NP (UNII: 4370DF050B)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- TALC (UNII: 7SEV7J4R1U)
* Please review the disclaimer below.
[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".