NDC 41595-5523 Pert Plus For Men Daily Dandruff
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What is NDC 41595-5523?
What are the uses for Pert Plus For Men Daily Dandruff?
Which are Pert Plus For Men Daily 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 For Men Daily 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)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS)
- POLYETHYLENE GLYCOL 7000 (UNII: Q0JET65GEL)
- 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 For Men Daily Dandruff?
- RxCUI: 1043145 - PERT PLUS 1 % Medicated Shampoo
- RxCUI: 1043145 - zinc pyrithione 10 MG/ML Medicated Shampoo [Pert Plus Dandruff]
- RxCUI: 1043145 - Pert Plus Dandruff 1 % Medicated Shampoo
- RxCUI: 1043145 - Pert Plus Dandruff 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".