NDC 68479-411 Clearing Mattifier
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 68479-411?
What are the uses for Clearing Mattifier?
Which are Clearing Mattifier 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 Clearing Mattifier 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:
- CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)
- DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)
- CETYL ETHYLHEXANOATE (UNII: 134647WMX4)
- WATER (UNII: 059QF0KO0R)
- ANNICKIA CHLORANTHA BARK (UNII: H70115MP4A)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- OLEANOLIC ACID (UNII: 6SMK8R7TGJ)
- HORSE CHESTNUT (UNII: 3C18L6RJAZ)
- CAMELLIA OLEIFERA LEAF (UNII: 5077EL0C60)
- CORALLINA OFFICINALIS (UNII: 4004498D06)
- CHAMOMILE (UNII: FGL3685T2X)
- GRAPE SEED OIL (UNII: 930MLC8XGG)
- SAFFLOWER OIL (UNII: 65UEH262IS)
- NIACINAMIDE (UNII: 25X51I8RD4)
- YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)
- ZINC GLUCONATE (UNII: U6WSN5SQ1Z)
- CAFFEINE (UNII: 3G6A5W338E)
- BIOTIN (UNII: 6SO6U10H04)
- AMMONIUM GLYCYRRHIZATE (UNII: 3VRD35U26C)
- STEARYL GLYCYRRHETINATE (UNII: 3YYE6VJS0P)
- SARCOSINE (UNII: Z711V88R5F)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
- PANTHENOL (UNII: WV9CM0O67Z)
- LAURYL PEG-9 POLYDIMETHYLSILOXYETHYL DIMETHICONE (UNII: 25G622K2RA)
- POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O)
- CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)
- BUTYLENE GLYCOL (UNII: 3XUS85K0RA)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
What is the NDC to RxNorm Crosswalk for Clearing Mattifier?
- RxCUI: 103568 - salicylic acid 2 % Topical Lotion
- RxCUI: 103568 - salicylic acid 20 MG/ML Topical Lotion
* 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".