NDC 53218-001 Total White Brightening
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 53218-001?
What are the uses for Total White Brightening?
Which are Total White Brightening UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Total White Brightening 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)
- COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL STEARATE (UNII: 5WX2EGD0DK)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- KOJIC ACID (UNII: 6K23F1TT52)
- CARROT SEED OIL (UNII: 595AO13F11)
- PENTETIC ACID (UNII: 7A314HQM0I)
- CORN OIL (UNII: 8470G57WFM)
- XANTHAN GUM (UNII: TTV12P4NEE)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .BETA.-CAROTENE (UNII: 01YAE03M7J)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- EDETATE SODIUM (UNII: MP1J8420LU)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- DMDM HYDANTOIN (UNII: BYR0546TOW)
- POLYETHYLENE GLYCOL 4500 (UNII: TVH7653921)
- SUGARCANE (UNII: 81H2R5AOH3)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON (UNII: 24RS0A988O)
- BILBERRY (UNII: 9P2U39H18W)
What is the NDC to RxNorm Crosswalk for Total White Brightening?
- RxCUI: 244594 - hydroquinone 2 % Topical Lotion
- RxCUI: 244594 - hydroquinone 20 MG/ML Topical Lotion
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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".