NDC 53208-530 Isaknox Tervina Lumiere White
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What is NDC 53208-530?
What are the uses for Isaknox Tervina Lumiere White?
Which are Isaknox Tervina Lumiere White UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHYL UNDECENOYL LEUCINATE (UNII: D7PH6N3IEI)
- METHYL UNDECENOYL LEUCINATE (UNII: D7PH6N3IEI) (Active Moiety)
Which are Isaknox Tervina Lumiere White 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- NEOPENTYL GLYCOL DICAPRATE (UNII: 77T908SE82)
- TREHALOSE (UNII: B8WCK70T7I)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- ETHYLPARABEN (UNII: 14255EXE39)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ISOBUTYLPARABEN (UNII: 0QQJ25X58G)
- C14-22 ALCOHOLS (UNII: B1K89384RJ)
- C12-20 ALKYL GLUCOSIDE (UNII: K67N5Z1RUA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- SQUALANE (UNII: GW89575KF9)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- TROMETHAMINE (UNII: 023C2WHX2V)
- EDETATE TRISODIUM (UNII: 420IP921MB)
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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".