NDC 55789-0101 Spf-40 Facial Moisturizer
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 55789-0101?
What are the uses for Spf-40 Facial Moisturizer?
Which are Spf-40 Facial Moisturizer UNII Codes?
The UNII codes for the active ingredients in this product are:
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Spf-40 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:
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
- CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)
- GLYCERIN (UNII: PDC6A3C0OX)
- HEXYL LAURATE (UNII: 4CG9F9W01Q)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)
- MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- SHEA BUTTER (UNII: K49155WL9Y)
- PANTHENOL (UNII: WV9CM0O67Z)
- MAGNESIUM ASPARTATE (UNII: R17X820ROL)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- JOJOBA OIL (UNII: 724GKU717M)
- TOCOPHEROL (UNII: R0ZB2556P8)
- COPPER GLUCONATE (UNII: RV823G6G67)
- HYALURONATE SODIUM (UNII: YSE9PPT4TH)
- PALMITOYL PENTAPEPTIDE-4 (UNII: KK181SM5JG)
- ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
- ALLANTOIN (UNII: 344S277G0Z)
- SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)
- LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- GREEN TEA LEAF (UNII: W2ZU1RY8B0)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
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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".