NDC 67938-0772 Ceramide Eyewish Eye Sunscreen Spf 10
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What is NDC 67938-0772?
What are the uses for Ceramide Eyewish Eye Sunscreen Spf 10?
Which are Ceramide Eyewish Eye Sunscreen Spf 10 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
Which are Ceramide Eyewish Eye Sunscreen Spf 10 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)
- HAMAMELIS VIRGINIANA LEAF WATER (UNII: 8FP93ED6H2)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- SQUALENE (UNII: 7QWM220FJH)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- PEG-100 STEARATE (UNII: YD01N1999R)
- GLYCERIN (UNII: PDC6A3C0OX)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- ALCOHOL (UNII: 3K9958V90M)
- TROLAMINE (UNII: 9O3K93S3TK)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- TOCOPHEROL (UNII: R0ZB2556P8)
- CARBOMER INTERPOLYMER TYPE A (55000 MPA.S) (UNII: 59TL3WG5CO)
- POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)
- SAXIFRAGA STOLONIFERA LEAF (UNII: O3TMV4903H)
- WINE GRAPE (UNII: 3GOV20705G)
- C13-14 ISOPARAFFIN (UNII: E4F12ROE70)
- DIAZOLIDINYL UREA (UNII: H5RIZ3MPW4)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CUCUMBER (UNII: YY7C30VXJT)
- RETINYL LINOLEATE (UNII: 61911N8D6W)
- EDETATE DISODIUM (UNII: 7FLD91C86K)
- OMEGA-3 FATTY ACIDS (UNII: 71M78END5S)
- LAURETH-7 (UNII: Z95S6G8201)
- CERAMIDE 3 (UNII: 4370DF050B)
- SODIUM METABISULFITE (UNII: 4VON5FNS3C)
- SODIUM SULFITE (UNII: VTK01UQK3G)
- SALVIA OFFICINALIS FLOWERING TOP (UNII: 48JCS720FN)
- GINKGO (UNII: 19FUJ2C58T)
- APPLE (UNII: B423VGH5S9)
- MORUS AUSTRALIS ROOT (UNII: 1VL55O45RF)
- SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- CENTELLA ASIATICA (UNII: 7M867G6T1U)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- OAT BRAN (UNII: KQX236OK4U)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- ECHINACEA PURPUREA (UNII: QI7G114Y98)
- VITIS VINIFERA SEED (UNII: C34U15ICXA)
- ERGOTHIONEINE (UNII: BDZ3DQM98W)
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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".