NDC 61016-0002 Antioxidant Day Spf 15
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 61016 - Columbia Cosmetics Manufacturing, Inc.
- 61016-0002 - Antioxidant Day Spf 15
Product Packages
NDC Code 61016-0002-2
Package Description: 59 mL in 1 BOTTLE
Product Details
What is NDC 61016-0002?
What are the uses for Antioxidant Day Spf 15?
Which are Antioxidant Day Spf 15 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Antioxidant Day 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)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- SQUALANE (UNII: GW89575KF9)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- SORBITAN MONOSTEARATE (UNII: NVZ4I0H58X)
- CYCLOMETHICONE 6 (UNII: XHK3U310BA)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALLANTOIN (UNII: 344S277G0Z)
- HEXYLENE GLYCOL (UNII: KEH0A3F75J)
- PANTHENOL (UNII: WV9CM0O67Z)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- TOCOPHEROL (UNII: R0ZB2556P8)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
* Please review the disclaimer below.
[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".