NDC 76214-005 Tomato Whitening Serum
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 76214-005?
What are the uses for Tomato Whitening Serum?
Which are Tomato Whitening Serum UNII Codes?
The UNII codes for the active ingredients in this product are:
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONE (UNII: 92RU3N3Y1O) (Active Moiety)
Which are Tomato Whitening 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERETH-26 (UNII: NNE56F2N14)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- ARBUTIN (UNII: C5INA23HXF)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- HYDROGENATED SOYBEAN LECITHIN (UNII: H1109Z9J4N)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POMEGRANATE (UNII: 56687D1Z4D)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- HONEY (UNII: Y9H1V576FH)
- HYDROXYETHYL UREA (UNII: MBQ7DDQ7AR)
- CHAENOMELES SPECIOSA FRUIT (UNII: 6S5Q1Q537Z)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- ARGININE (UNII: 94ZLA3W45F)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
What is the NDC to RxNorm Crosswalk for Tomato Whitening Serum?
- 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".