NDC 78493-001 Sun-kissed Suncream
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 78493-001?
What are the uses for Sun-kissed Suncream?
Which are Sun-kissed Suncream UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC CATION (UNII: 13S1S8SF37) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- OCTISALATE (UNII: 4X49Y0596W)
- OCTISALATE (UNII: 4X49Y0596W) (Active Moiety)
Which are Sun-kissed Suncream 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)
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)
- DIMETHICONE/PEG-10/15 CROSSPOLYMER (UNII: 21AS8B1BSS)
- DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)
- IODOPROPYNYL BUTYLCARBAMATE (UNII: 603P14DHEB)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- DIPROPYLENE GLYCOL (UNII: E107L85C40)
- CORN OIL (UNII: 8470G57WFM)
- TOCOPHEROL (UNII: R0ZB2556P8)
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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".