NDC 76214-007 Omija Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76214 - Skinfood Co., Ltd.
- 76214-007 - Omija Whitening
Product Packages
NDC Code 76214-007-01
Package Description: 50 g in 1 CARTON
Product Details
What is NDC 76214-007?
What are the uses for Omija Whitening?
Which are Omija Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Omija 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)
- SCHISANDRA CHINENSIS FRUIT (UNII: ABS794681C)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ISOTRIDECYL ISONONANOATE (UNII: WEF51750MT)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SALIX NIGRA BARK (UNII: QU52J3A5B3)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- MAACKIA FLORIBUNDA STEM (UNII: 84UXW52K8Y)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SORBITOL (UNII: 506T60A25R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CHAMOMILE (UNII: FGL3685T2X)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- SUCROSE LAURATE (UNII: 05Q7CD0E49)
- MORUS ALBA ROOT (UNII: CST1G9BZGD)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- CERAMIDE 3 (UNII: 4370DF050B)
- SODIUM ASCORBYL PHOSPHATE (UNII: 836SJG51DR)
What is the NDC to RxNorm Crosswalk for Omija Whitening?
- RxCUI: 1116731 - dimethicone 4 % Topical Cream
- RxCUI: 1116731 - dimethicone 40 MG/ML Topical Cream
* 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".