NDC 69299-302 Dr. Throwers Skin Lightening Moisturizing
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 69299-302?
What are the uses for Dr. Throwers Skin Lightening Moisturizing?
Which are Dr. Throwers Skin Lightening Moisturizing UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Dr. Throwers Skin Lightening Moisturizing 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)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- MINERAL OIL (UNII: T5L8T28FGP)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARETH-22 (UNII: 28VZG1E234)
- STARCH, POTATO (UNII: 8I089SAH3T)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S) (UNII: 587WKM3S9Q)
- LANOLIN (UNII: 7EV65EAW6H)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- GRAPEFRUIT PEEL (UNII: 3582N05Q44)
- EDETATE SODIUM TETRAHYDRATE (UNII: L13NHD21X6)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
What is the NDC to RxNorm Crosswalk for Dr. Throwers Skin Lightening Moisturizing?
- 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".