NDC 65113-8401 Skin Lightening Complex
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 65113-8401?
What are the uses for Skin Lightening Complex?
Which are Skin Lightening Complex UNII Codes?
The UNII codes for the active ingredients in this product are:
- HYDROQUINONE (UNII: XV74C1N1AE)
- PHENOL (UNII: 339NCG44TV) (Active Moiety)
Which are Skin Lightening Complex 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)
- GLYCOLIC ACID (UNII: 0WT12SX38S)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- C12-15 ALKYL BENZOATE (UNII: A9EJ3J61HQ)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- MYRISTYL ALCOHOL (UNII: V42034O9PU)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- POLYOXYL 100 STEARATE (UNII: YD01N1999R)
- LACTIC ACID (UNII: 33X04XA5AT)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- ARCTOSTAPHYLOS UVA-URSI LEAF (UNII: 3M5V3D1X36)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
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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".