NDC 64141-112 Extra Repair Moisturing Balm Spf 25
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 64141-112?
Which are Extra Repair Moisturing Balm Spf 25 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
Which are Extra Repair Moisturing Balm Spf 25 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)
- SHEA BUTTER (UNII: K49155WL9Y)
- PROPANEDIOL (UNII: 5965N8W85T)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)
- SUCROSE (UNII: C151H8M554)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- BLACK OLIVE (UNII: 2M6QWV94OC)
- CLARY SAGE (UNII: U3HSK5JC0Q)
- EPILOBIUM ANGUSTIFOLIUM FLOWERING TOP (UNII: 08H094218D)
- WHEAT BRAN (UNII: 6L966A1IMR)
- PEA (UNII: W4X7H8GYFM)
- BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
- ROSEMARY (UNII: IJ67X351P9)
- EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)
- PELARGONIUM GRAVEOLENS FLOWERING TOP (UNII: 1P36QZP48P)
- CITRUS MAXIMA FRUIT RIND (UNII: 5NX3G75CA6)
- CITRUS AURANTIUM FLOWER OIL (UNII: D4BGE91OXH)
- CHAMAEMELUM NOBILE (UNII: 7NF3GE7IWR)
- WHEY (UNII: 8617Z5FMF6)
- CHOLESTEROL (UNII: 97C5T2UQ7J)
- LINOLEIC ACID (UNII: 9KJL21T0QJ)
- CAFFEINE (UNII: 3G6A5W338E)
- ACETYL HEXAPEPTIDE-3 (UNII: L4EL31FWIL)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- PEG-40 STEARATE (UNII: ECU18C66Q7)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DIHEXADECYL PHOSPHATE (UNII: 2V6E5WN99N)
- CETETH-10 PHOSPHATE (UNII: 4E05O5N49G)
- LAURETH-7 (UNII: Z95S6G8201)
- GLUCOSAMINE HYDROCHLORIDE (UNII: 750W5330FY)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- XANTHAN GUM (UNII: TTV12P4NEE)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- EDETATE SODIUM (UNII: MP1J8420LU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".