NDC 13537-022 Lbel Effet Parfait Mineral
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 13537 - Ventura Corporation Ltd.
- 13537-022 - Lbel
Product Packages
NDC Code 13537-022-02
Package Description: 1 CONTAINER in 1 CARTON / 10 g in 1 CONTAINER (13537-022-01)
Product Details
What is NDC 13537-022?
What are the uses for Lbel Effet Parfait Mineral?
Which are Lbel Effet Parfait Mineral UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
- OXYBENZONE (UNII: 95OOS7VE0Y)
- OXYBENZONE (UNII: 95OOS7VE0Y) (Active Moiety)
- ZINC OXIDE (UNII: SOI2LOH54Z)
- ZINC OXIDE (UNII: SOI2LOH54Z) (Active Moiety)
- OCTINOXATE (UNII: 4Y5P7MUD51)
- OCTINOXATE (UNII: 4Y5P7MUD51) (Active Moiety)
Which are Lbel Effet Parfait Mineral 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:
- MICA (UNII: V8A1AW0880)
- STARCH, CORN (UNII: O8232NY3SJ)
- ZINC STEARATE (UNII: H92E6QA4FV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)
- JOJOBA OIL (UNII: 724GKU717M)
- GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- CAPRYLYL GLYCOL (UNII: 00YIU5438U)
- CHLORPHENESIN (UNII: I670DAL4SZ)
- CARNOSINE (UNII: 8HO6PVN24W)
- ALANYL-GLUTAMINE (UNII: U5JDO2770Z)
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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".