NDC 69423-606 Olay Regenerist Vitamin C Plus Peptide 24 Hydrating Moisturizer With Sunscreen Broad Spectrum Spf 30
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69423 - The Procter & Gamble Manufacturing Company
- 69423-606 - Olay Regenerist Vitamin C Plus Peptide 24 Hydrating Moisturizer
Product Packages
NDC Code 69423-606-50
Package Description: 1 BOTTLE, PUMP in 1 CARTON / 50 mL in 1 BOTTLE, PUMP
Product Details
What is NDC 69423-606?
What are the uses for Olay Regenerist Vitamin C Plus Peptide 24 Hydrating Moisturizer With Sunscreen Broad Spectrum Spf 30?
Which are Olay Regenerist Vitamin C Plus Peptide 24 Hydrating Moisturizer With Sunscreen Broad Spectrum Spf 30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
Which are Olay Regenerist Vitamin C Plus Peptide 24 Hydrating Moisturizer With Sunscreen Broad Spectrum Spf 30 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:
- 3-O-ETHYL ASCORBIC ACID (UNII: 6MW60CB71P)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)
- PALMITIC ACID (UNII: 2V16EO95H1)
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- NIACINAMIDE (UNII: 25X51I8RD4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PANTHENOL (UNII: WV9CM0O67Z)
- STARCH, CORN (UNII: O8232NY3SJ)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- PEG-100 STEARATE (UNII: YD01N1999R)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- DOCOSANOL (UNII: 9G1OE216XY)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- DIMETHICONOL GUM (UNII: 4MJ9GU3T1P)
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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".