NDC 67938-1436 Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67938 - Elizabeth Arden, Inc
- 67938-1436 - Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11
Product Characteristics
Product Packages
NDC Code 67938-1436-1
Package Description: 1 CONTAINER in 1 BOX / 8.33 g in 1 CONTAINER (67938-1436-2)
Product Details
What is NDC 67938-1436?
What are the uses for Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11?
Which are Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11 UNII Codes?
The UNII codes for the active ingredients in this product are:
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Active Moiety)
Which are Pure Finish Mineral Powder Foundation Spf 20 Pure Finish 11 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)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- ZINC STEARATE (UNII: H92E6QA4FV)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SQUALANE (UNII: GW89575KF9)
- MAGNESIUM MYRISTATE (UNII: Z1917F0578)
- SEA SALT (UNII: 87GE52P74G)
- STARCH, RICE (UNII: 4DGK8B7I3S)
- ALUMINUM OXIDE (UNII: LMI26O6933)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- ALOE VERA LEAF (UNII: ZY81Z83H0X)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- ASCORBYL PALMITATE (UNII: QN83US2B0N)
- BUTYLPARABEN (UNII: 3QPI1U3FV8)
- ALPHA-TOCOPHEROL (UNII: H4N855PNZ1)
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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".