NDC 76354-205 Mineral Blemish Kit
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76354 - J. A. Cosmetics U.s. Inc
- 76354-205 - Mineral Blemish Kit
Product Packages
NDC Code 76354-205-21
Package Description: 3.3 g in 1 BOX
Product Details
What is NDC 76354-205?
What are the uses for Mineral Blemish Kit?
Which are Mineral Blemish Kit UNII Codes?
The UNII codes for the active ingredients in this product are:
- SULFUR (UNII: 70FD1KFU70)
- SULFUR (UNII: 70FD1KFU70) (Active Moiety)
Which are Mineral Blemish Kit 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)
- BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)
- ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)
- MINERAL OIL (UNII: T5L8T28FGP)
- TEA TREE OIL (UNII: VIF565UC2G)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Mineral Blemish Kit?
- RxCUI: 1191710 - sulfur 3 % Topical Powder
- RxCUI: 1191710 - sulfur 0.03 MG/MG Topical Powder
* Please review the disclaimer below.
[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".