NDC 68723-330 Dermesse Sunscreen Spf30
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 68723-330?
What are the uses for Dermesse Sunscreen Spf30?
Which are Dermesse Sunscreen Spf30 UNII Codes?
The UNII codes for the active ingredients in this product are:
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Dermesse Sunscreen Spf30 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)
- ISOCETYL STEARATE (UNII: 3RJ7186O9W)
- SORBITOL (UNII: 506T60A25R)
- CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
- POLYOXYL 20 CETOSTEARYL ETHER (UNII: YRC528SWUY)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- ACETYL HEXAPEPTIDE-8 (UNII: L4EL31FWIL)
- ALCOHOL (UNII: 3K9958V90M)
- DIMETHICONE 350 (UNII: 2Y53S6ATLU)
- OCTISALATE (UNII: 4X49Y0596W)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- METHICONE (20 CST) (UNII: 6777U11MKT)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- TROLAMINE (UNII: 9O3K93S3TK)
- STEARIC ACID (UNII: 4ELV7Z65AP)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
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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".