NDC 59779-601 Illuminating Daily Moisturizer Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 59779 - Cvs Pharmacy Inc
- 59779-601 - Illuminating Daily Moisturizer
Product Packages
NDC Code 59779-601-04
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 118 mL in 1 BOTTLE, PUMP (59779-601-00)
NDC Code 59779-601-05
Package Description: 118 mL in 1 BOTTLE, PLASTIC
Product Details
What is NDC 59779-601?
What are the uses for Illuminating Daily Moisturizer Spf 15?
Which are Illuminating Daily Moisturizer Spf 15 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)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Illuminating Daily Moisturizer Spf 15 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)
- ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)
- DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SOYBEAN (UNII: L7HT8F1ZOD)
- GLYCERIN (UNII: PDC6A3C0OX)
- BIS-PHENYLPROPYL DIMETHICONE (15 CST) (UNII: 4836494CFT)
- ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- PANTHENOL (UNII: WV9CM0O67Z)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- ACRYLIC ACID/ETHYLENE COPOLYMER (600 MPA.S) (UNII: 1PEZ3NLY6I)
- DOCOSANOL (UNII: 9G1OE216XY)
- STEARETH-2 (UNII: V56DFE46J5)
- STEARETH-21 (UNII: 53J3F32P58)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- NYLON-12 (UNII: 446U8J075B)
- ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- LAURETH-7 (UNII: Z95S6G8201)
- BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MICA (UNII: V8A1AW0880)
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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".