NDC 61671-004 Face Moisturiser
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 61671-004?
What are the uses for Face Moisturiser?
Which are Face Moisturiser 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)
Which are Face Moisturiser 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)
- CETEARYL OLIVATE (UNII: 58B69Q84JO)
- CYCLOMETHICONE (UNII: NMQ347994Z)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- ULVA COMPRESSA (UNII: SXZ209FM33)
- FUCUS SERRATUS (UNII: V8K40WNW5B)
- GLYCERIN (UNII: PDC6A3C0OX)
- ISOHEXADECANE (UNII: 918X1OUF1E)
- LACTIC ACID (UNII: 33X04XA5AT)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DULSE (UNII: 7832HOY4ZQ)
- PANTHENOL (UNII: WV9CM0O67Z)
- PENTYLENE GLYCOL (UNII: 50C1307PZG)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- SERINE (UNII: 452VLY9402)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM LACTATE (UNII: TU7HW0W0QT)
- SORBITAN OLIVATE (UNII: MDL271E3GR)
- SORBITOL (UNII: 506T60A25R)
- METHACRYLATE/METHOXY PEG-10 MALEATE/STYRENE COPOLYMER (UNII: 39DK5WQ2PR)
- UREA (UNII: 8W8T17847W)
- XANTHAN GUM (UNII: TTV12P4NEE)
- SODIUM ACRYLATE/SODIUM ACRYLOYLDIMETHYLTAURATE COPOLYMER (4000000 MW) (UNII: 1DXE3F3OZX)
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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".