NDC 42743-4700 American Crew Anti-dandruff Plus Sebum Control
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 42743-4700?
What are the uses for American Crew Anti-dandruff Plus Sebum Control?
Which are American Crew Anti-dandruff Plus Sebum Control UNII Codes?
The UNII codes for the active ingredients in this product are:
- PYRITHIONE ZINC (UNII: R953O2RHZ5)
- PYRITHIONE ZINC (UNII: R953O2RHZ5) (Active Moiety)
Which are American Crew Anti-dandruff Plus Sebum Control 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:
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG-12 DIMETHICONE (300 CST) (UNII: ZEL54N6W95)
- DI-PPG-2 MYRETH-10 ADIPATE (UNII: 4IN301M0KJ)
- TROLAMINE (UNII: 9O3K93S3TK)
- HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%) (UNII: R33S7TK2EP)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600000 MW) (UNII: 0L414VCS5Y)
- TEA TREE OIL (UNII: VIF565UC2G)
- PEPPERMINT OIL (UNII: AV092KU4JH)
- ROSEMARY (UNII: IJ67X351P9)
- SAGE (UNII: 065C5D077J)
- SODIUM ACETATE (UNII: 4550K0SC9B)
- LIMONENE, (+)- (UNII: GFD7C86Q1W)
- PHENOXYETHANOL (UNII: HIE492ZZ3T)
- ETHYLPARABEN (UNII: 14255EXE39)
- METHYLPARABEN (UNII: A2I8C7HI9T)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
What is the NDC to RxNorm Crosswalk for American Crew Anti-dandruff Plus Sebum Control?
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Conditioner
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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".