Label: PERT PLUS DANDRUFF PLUS- pyrithione zinc shampoo, suspension
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Contains inactivated NDC Code(s)
NDC Code(s): 41595-5526-3 - Packager: Idelle Labs, Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- 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, glycerin (and) Avena Sativa (oat) kernel extract, bisabolol, fragrance, Melaleuca Alternifolia (tea tree) leaf oil, Carthamus Tinctorius (safflower) seed oil, and Mentha Arvensis (wild mint) leaf extract, cetyl alcohol, cocamide MEA, sodium chloride, 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 DANDRUFF PLUS
pyrithione zinc shampoo, suspensionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41595-5526 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 0.45 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 CITRATE (UNII: 1Q73Q2JULR) SODIUM BENZOATE (UNII: OJ245FE5EU) POLYETHYLENE GLYCOL 7000 (UNII: Q0JET65GEL) POLYQUATERNIUM-10 (400 CPS AT 2%) (UNII: HB1401PQFS) BENZYL ALCOHOL (UNII: LKG8494WBH) SODIUM CHLORIDE (UNII: 451W47IQ8X) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA) METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) D&C YELLOW NO. 10 (UNII: 35SW5USQ3G) TEA TREE OIL (UNII: VIF565UC2G) SAFFLOWER OIL (UNII: 65UEH262IS) MINT (UNII: FV98Z8GITP) OAT (UNII: Z6J799EAJK) LEVOMENOL (UNII: 24WE03BX2T) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41595-5526-3 400 mL in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC MONOGRAPH FINAL part358H 12/01/2009 Labeler - Idelle Labs, Ltd (128822926) Registrant - Idelle Labs, Ltd (128822926) Establishment Name Address ID/FEI Business Operations Body Blue 2006 Inc. 243094112 MANUFACTURE