Label: PERT PLUS FOR MEN DAILY DANDRUFF- pyrithione zinc shampoo, suspension
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Contains inactivated NDC Code(s)
NDC Code(s): 41595-5523-7 - Packager: Idelle Labs, Ltd
- Category: HUMAN OTC DRUG LABEL
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated December 29, 2010
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Pert Plus for Men Daily Dandruff
- Active Ingredient
- Purpose:
- Uses
- Warning:
- When using this product
- Stop use and ask a doctor
- Keep this and all drugs out of reach of children.
- Directions:
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Inactive Ingredients:
Water, ammonium laureth sulfate, ammonium lauryl sulfate, glycol distearate, dimethicone, hydrolyzed vegetable protein PG-propyl silanetriol, cetyl alcohol, cocamide MEA, sodium chloride, fragrance, guar hydroxypropyltrimonium chloride, hydrogenated polydecene, sodium citrate, sodium benzoate, polyquaternium 10, PEG-7M, trimethylolpropane tricaprylate/tricaprate, citric acid, benzyl alcohol, methylchloroisothiazolinone, methylisothiazolinone, ammonium xylene sulfonate, D & C Yellow No. 10, FD & C Blue No. 1.
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Questions?
1-800-487-7273 or visit us at www.pertplus.com
©2011 Idelle Labs, Ltd. All rights reserved
Made in the Canada and distributed by Idelle Labs, Ltd., El Paso, TX 79912 - PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PERT PLUS FOR MEN DAILY DANDRUFF
pyrithione zinc shampoo, suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41595-5523 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 mL in 100 mL Inactive Ingredients Ingredient Name Strength 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) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41595-5523-7 354 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part358H 04/01/2010 Labeler - Idelle Labs, Ltd (128822926) Registrant - Idelle Labs, Ltd (128822926) Establishment Name Address ID/FEI Business Operations Body Blue 2006 Inc. 243094112 MANUFACTURE