NDC 41163-356 Equaline All Day Moisturizer
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What is NDC 41163-356?
What are the uses for Equaline All Day Moisturizer?
Which are Equaline All Day Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
- AVOBENZONE (UNII: G63QQF2NOX)
- AVOBENZONE (UNII: G63QQF2NOX) (Active Moiety)
- HOMOSALATE (UNII: V06SV4M95S)
- HOMOSALATE (UNII: V06SV4M95S) (Active Moiety)
- OCTOCRYLENE (UNII: 5A68WGF6WM)
- OCTOCRYLENE (UNII: 5A68WGF6WM) (Active Moiety)
Which are Equaline All Day Moisturizer 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:
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- DOCOSANOL (UNII: 9G1OE216XY)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- DIMETHICONOL (2000 CST) (UNII: T74O12AN6Y)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ETHYLPARABEN (UNII: 14255EXE39)
- GLYCERIN (UNII: PDC6A3C0OX)
- HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (45000 MPA.S AT 1%) (UNII: 86FQE96TZ4)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PANTHENOL (UNII: WV9CM0O67Z)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- NIACINAMIDE (UNII: 25X51I8RD4)
- POLYETHYLENE GLYCOL 200 (UNII: R95B8J264J)
- PEG-4 DILAURATE (UNII: KCR71CW036)
- PEG-4 LAURATE (UNII: AYF4VM3N1Z)
- PEG-100 STEARATE (UNII: YD01N1999R)
- HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- WATER (UNII: 059QF0KO0R)
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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".