NDC 20151-102 Lightening Brightening Moisturizing Serum
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 20151-102?
What are the uses for Lightening Brightening Moisturizing Serum?
Which are Lightening Brightening Moisturizing Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- GLYCERIN (UNII: PDC6A3C0OX)
- GLYCERIN (UNII: PDC6A3C0OX) (Active Moiety)
Which are Lightening Brightening Moisturizing Serum 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:
- XANTHAN GUM (UNII: TTV12P4NEE)
- MORUS AUSTRALIS ROOT (UNII: 1VL55O45RF)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- WINE GRAPE (UNII: 3GOV20705G)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- WATER (UNII: 059QF0KO0R)
- SAXIFRAGA STOLONIFERA LEAF (UNII: O3TMV4903H)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- TETRASODIUM GLUTAMATE DIACETATE (UNII: 5EHL50I4MY)
- ERYTHRITOL (UNII: RA96B954X6)
- DULSE (UNII: 7832HOY4ZQ)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- ASCORBYL GLUCOSIDE (UNII: 2V52R0NHXW)
- NONAPEPTIDE-1 (UNII: 64W45420K5)
- DEXTRAN 40 (UNII: K3R6ZDH4DU)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- PROPANEDIOL (UNII: 5965N8W85T)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- HOMARINE HYDROCHLORIDE (UNII: 8866LNG61N)
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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".