NDC 54272-301 Brighten Lightening
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 54272-301?
What are the uses for Brighten Lightening?
Which are Brighten Lightening UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Brighten Lightening 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)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ALLANTOIN (UNII: 344S277G0Z)
- AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
- GLYCERIN (UNII: PDC6A3C0OX)
- OAT (UNII: Z6J799EAJK)
- ANGELICA SINENSIS WHOLE (UNII: 697D19QDBN)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- 10-HYDROXYDECANOIC ACID (UNII: NP03XO416B)
- 1,10-DECANEDIOL (UNII: 5I577UDK52)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- LACTIC ACID (UNII: 33X04XA5AT)
- GLYCERETH-7 TRIMETHYL ETHER (UNII: XMC7402M60)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- XANTHAN GUM (UNII: TTV12P4NEE)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
What is the NDC to RxNorm Crosswalk for Brighten Lightening?
- RxCUI: 199176 - hydroquinone 2 % Topical Gel
- RxCUI: 199176 - hydroquinone 0.02 MG/MG Topical Gel
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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".