NDC 62673-163 Enhanced Facial Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 62673-163?
What are the uses for Enhanced Facial Moisturizer?
Which are Enhanced Facial Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
Which are Enhanced Facial 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:
- WATER (UNII: 059QF0KO0R)
- CORN OIL (UNII: 8470G57WFM)
- SOYBEAN OIL (UNII: 241ATL177A)
- DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- LAURETH-7 (UNII: Z95S6G8201)
- STEARETH-21 (UNII: 53J3F32P58)
- GLYCERIN (UNII: PDC6A3C0OX)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- MYRISTYL MYRISTATE (UNII: 4042ZC00DY)
- PETROLATUM (UNII: 4T6H12BN9U)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- PANTOTHENIC ACID (UNII: 19F5HK2737)
- STEARETH-2 (UNII: V56DFE46J5)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- TROLAMINE (UNII: 9O3K93S3TK)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
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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".