NDC 73618-001 E-ko Skin Care Spf 50
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 73618-001?
What are the uses for E-ko Skin Care Spf 50?
Which are E-ko Skin Care Spf 50 UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
Which are E-ko Skin Care Spf 50 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)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- CAPRYLYL CAPRYLATE/CAPRATE (UNII: 22MCG4RSMR)
- MACADAMIA OIL (UNII: 515610SU8C)
- KUKUI NUT OIL (UNII: TP11QR7B8R)
- POLYGLYCERYL-2 OLEATE (UNII: 5759J47SAM)
- POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)
- GLYCERIN (UNII: PDC6A3C0OX)
- COCONUT OIL (UNII: Q9L0O73W7L)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)
- HYDROGENATED METHYL ABIETATE (UNII: A23O709X8O)
- GALACTOARABINAN (UNII: SL4SX1O487)
- PROPANEDIOL (UNII: 5965N8W85T)
- POLYGLYCERYL-2 STEARATE (UNII: 253MC0P0YV)
- COFFEA ARABICA FRUIT (UNII: HOX6BEK27Q)
- NONI FRUIT JUICE (UNII: 6ULF85Z07J)
- ARTHROSPIRA PLATENSIS (UNII: 9L3TIH1UUE)
- RICE BRAN (UNII: R60QEP13IC)
- ROSEMARY (UNII: IJ67X351P9)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- APRICOT (UNII: 269CJD5GZ9)
- VANILLA BEAN (UNII: Q74T35078H)
- MUSKMELON (UNII: ZV095H5633)
- CRANBERRY (UNII: 0MVO31Q3QS)
- BANANA (UNII: 4AJZ4765R9)
- SANDALWOOD (UNII: 3641YW25N2)
- ARABICA COFFEE BEAN (UNII: 3SW678MX72)
- APPLE (UNII: B423VGH5S9)
- COCONUT (UNII: 3RT3536DHY)
- SUNFLOWER OIL (UNII: 3W1JG795YI)
- TOCOPHEROL (UNII: R0ZB2556P8)
- PLUMERIA ALBA FLOWER (UNII: LGC8P2PC4H)
- KAOLIN (UNII: 24H4NWX5CO)
- 1,2-HEXANEDIOL (UNII: TR046Y3K1G)
- CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)
* Please review the disclaimer below.
[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".