NDC 70969-101 Ginseng Whitening
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 70969-101?
What are the uses for Ginseng Whitening?
Which are Ginseng Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- NIACINAMIDE (UNII: 25X51I8RD4)
- NIACINAMIDE (UNII: 25X51I8RD4) (Active Moiety)
Which are Ginseng Whitening 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)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- GLYCERIN (UNII: PDC6A3C0OX)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- GLYCERYL OLEATE (UNII: 4PC054V79P)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- EGG PHOSPHOLIPIDS (UNII: 1Z74184RGV)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- TRANEXAMIC ACID (UNII: 6T84R30KC1)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- GINSENOSIDES (UNII: 3K198YD54P)
- PEG-100 STEARATE (UNII: YD01N1999R)
- POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)
- GRAPEFRUIT (UNII: O82C39RR8C)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
- ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
- PURSLANE (UNII: M6S840WXG5)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
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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".