NDC 76354-201 Clarifying Pressed Powder
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 76354 - J. A. Cosmetics U.s. Inc
- 76354-201 - Clarifying Pressed Powder
Product Packages
NDC Code 76354-201-51
Package Description: 1 TUBE in 1 BOX / 30 g in 1 TUBE (76354-201-11)
Product Details
What is NDC 76354-201?
What are the uses for Clarifying Pressed Powder?
Which are Clarifying Pressed Powder UNII Codes?
The UNII codes for the active ingredients in this product are:
- SALICYLIC ACID (UNII: O414PZ4LPZ)
- SALICYLIC ACID (UNII: O414PZ4LPZ) (Active Moiety)
Which are Clarifying Pressed Powder 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:
- TALC (UNII: 7SEV7J4R1U)
- MICA (UNII: V8A1AW0880)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- ETHYLHEXYL PALMITATE (UNII: 2865993309)
- MINERAL OIL (UNII: T5L8T28FGP)
- POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
- SODIUM DEHYDROACETATE (UNII: 8W46YN971G)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FERROSOFERRIC OXIDE (UNII: XM0M87F357)
What is the NDC to RxNorm Crosswalk for Clarifying Pressed Powder?
- RxCUI: 1191691 - salicylic acid 1 % Topical Powder
- RxCUI: 1191691 - salicylic acid 0.01 MG/MG Topical Powder
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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".