NDC 68479-213 Purelight Spf50
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68479-213?
What are the uses for Purelight Spf50?
Which are Purelight Spf50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Purelight Spf50 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)
- CARTHAMUS TINCTORIUS SEED OLEOSOMES (UNII: 9S60Q72309)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- DIMETHYL CAPRAMIDE (UNII: O29Y6X2JEZ)
- CANANGA OIL (UNII: 8YOY78GNNX)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- LAVANDIN OIL (UNII: 9RES347CKG)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- LAMINARIA OCHROLEUCA (UNII: 4R2124HE76)
- DULSE (UNII: 7832HOY4ZQ)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- ZINC GLYCINATE (UNII: 681VJX72FE)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- BUTYLENE GLYCOL BEHENATE (UNII: X0IW5BP6ZL)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".