NDC 59151-645 Skin And Scalp
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 59151-645?
What are the uses for Skin And Scalp?
Which are Skin And Scalp UNII Codes?
The UNII codes for the active ingredients in this product are:
- COAL TAR (UNII: R533ESO2EC)
- COAL TAR (UNII: R533ESO2EC) (Active Moiety)
Which are Skin And Scalp 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:
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- COCAMIDOPROPYL DIMETHYLAMINE PROPIONATE (UNII: 83750MLC4A)
- PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
- CAMPHOR (NATURAL) (UNII: N20HL7Q941)
- JOJOBA OIL (UNII: 724GKU717M)
- BIOTIN (UNII: 6SO6U10H04)
- POLYSORBATE 80 (UNII: 6OZP39ZG8H)
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- BENZOIC ACID (UNII: 8SKN0B0MIM)
- PROPYLPARABEN (UNII: Z8IX2SC1OH)
- MENTHOL (UNII: L7T10EIP3A)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)
- VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
What is the NDC to RxNorm Crosswalk for Skin And Scalp?
- RxCUI: 1812569 - coal tar 1.7 % Medicated Shampoo
- RxCUI: 1812569 - coal tar 17 MG/ML Medicated Shampoo
* 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".