NDC 78863-1050 Double White
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 78863-1050?
What are the uses for Double White?
Which are Double White UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- HYDROQUINONE (UNII: XV74C1N1AE) (Active Moiety)
Which are Double White 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:
- PROPANEDIOL (UNII: 5965N8W85T)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- AZELAIC ACID (UNII: F2VW3D43YT)
- WATER (UNII: 059QF0KO0R)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ALCOHOL (UNII: 3K9958V90M)
- ALPHA-ARBUTIN (UNII: 72VUP07IT5)
- DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
- STRONTIUM CHLORIDE HEXAHYDRATE (UNII: O09USB7Z44)
- GLYCERIN (UNII: PDC6A3C0OX)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- ANHYDROUS DEXTROSE (UNII: 5SL0G7R0OK)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETYL PALMITATE (UNII: 5ZA2S6B08X)
- DIMETHYL ISOSORBIDE (UNII: SA6A6V432S)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- DOCOSANOL (UNII: 9G1OE216XY)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- XYLITYLGLUCOSIDE (UNII: O0IEZ166FB)
- ANHYDROXYLITOL (UNII: 8XWR7NN42F)
- XYLITOL (UNII: VCQ006KQ1E)
- PROPOLIS WAX (UNII: 6Y8XYV2NOF)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- PUMMELO (UNII: ET1TN5W71X)
- LEMON OIL (UNII: I9GRO824LL)
- PHYTATE SODIUM (UNII: 88496G1ERL)
- POTASSIUM AZELOYL DIGLYCINATE (UNII: N02RVN6NYP)
* 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".