NDC 76214-023 Fresh Juice C Whitening Care
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76214 - Skinfood Co., Ltd.
- 76214-023 - Fresh Juice C
Product Packages
NDC Code 76214-023-01
Package Description: 50 g in 1 BOTTLE
Product Details
What is NDC 76214-023?
What are the uses for Fresh Juice C Whitening Care?
Which are Fresh Juice C Whitening Care UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Fresh Juice C Whitening Care 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)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ARBUTIN (UNII: C5INA23HXF)
- HONEY (UNII: Y9H1V576FH)
- NIACINAMIDE (UNII: 25X51I8RD4)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- TROLAMINE (UNII: 9O3K93S3TK)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- KIWI FRUIT (UNII: 71ES77LGJC)
- ORANGE (UNII: 5EVU04N5QU)
- LEMON (UNII: 24RS0A988O)
- GLYCYRRHIZA GLABRA (UNII: 2788Z9758H)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- POLYETHYLENE GLYCOL 7000 (UNII: Q0JET65GEL)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- PUMPKIN SEED (UNII: GH30P1VXK2)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MEADOWFOAM SEED OIL (UNII: 412ZHA4T4Y)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
What is the NDC to RxNorm Crosswalk for Fresh Juice C Whitening Care?
- RxCUI: 200010 - dimethicone 1 % Topical Cream
- RxCUI: 200010 - dimethicone 10 MG/ML Topical Cream
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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".