NDC 41595-8001 Pert Plus 2 In 1 Anti-dandruff
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What is NDC 41595-8001?
What are the uses for Pert Plus 2 In 1 Anti-dandruff?
Which are Pert Plus 2 In 1 Anti-dandruff 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 Pert Plus 2 In 1 Anti-dandruff 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:
- WATER (UNII: 059QF0KO0R)
- AMMONIUM LAURETH-5 SULFATE (UNII: 43ZIH89I48)
- AMMONIUM LAURYL SULFATE (UNII: Q7AO2R1M0B)
- GLYCOL DISTEARATE (UNII: 13W7MDN21W)
- DIMETHICONE (UNII: 92RU3N3Y1O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- COCO MONOETHANOLAMIDE (UNII: C80684146D)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
- HYDROGENATED POLYDECENE (550 MW) (UNII: U333RI6EB7)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- POLYETHYLENE GLYCOL 7000 (UNII: Q0JET65GEL)
- TRIMETHYLOLPROPANE TRICAPRYLATE/TRICAPRATE (UNII: N1TRQ06KVJ)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- BENZYL ALCOHOL (UNII: LKG8494WBH)
- METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
- METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
- D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
What is the NDC to RxNorm Crosswalk for Pert Plus 2 In 1 Anti-dandruff?
- RxCUI: 1043244 - head & shoulders 1 % Medicated Shampoo
- RxCUI: 1043244 - zinc pyrithione 10 MG/ML Medicated Shampoo [Head & Shoulders]
- RxCUI: 1043244 - Head & Shoulders 1 % Medicated Shampoo
- RxCUI: 1043244 - Head & Shoulders 10 MG/ML Medicated Shampoo
- RxCUI: 209884 - zinc pyrithione 1 % Medicated Shampoo
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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".