NDC 37000-355 Olay Total Effects Cc Tone Correcting Broad Spectrum Spf 15 Light To Medium
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 37000 - The Procter & Gamble Manufacturing Company
- 37000-355 - Olay Total Effects Cc Tone Correcting
Product Packages
NDC Code 37000-355-50
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 37000-355?
What are the uses for Olay Total Effects Cc Tone Correcting Broad Spectrum Spf 15 Light To Medium?
Which are Olay Total Effects Cc Tone Correcting Broad Spectrum Spf 15 Light To Medium UNII Codes?
The UNII codes for the active ingredients in this product are:
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Olay Total Effects Cc Tone Correcting Broad Spectrum Spf 15 Light To Medium 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)
- GLYCERIN (UNII: PDC6A3C0OX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- N-ACETYLGLUCOSAMINE (UNII: V956696549)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTHENOL (UNII: WV9CM0O67Z)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- DOCOSANOL (UNII: 9G1OE216XY)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- ETHYLPARABEN (UNII: 14255EXE39)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J)
- POLYACRYLAMIDE (1300000 MW) (UNII: SC5Y4X78TG)
- TROLAMINE (UNII: 9O3K93S3TK)
- CARBOXYPOLYMETHYLENE (UNII: 0A5MM307FC)
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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".