PERT PLUS FOR MEN DAILY DANDRUFF- pyrithione zinc shampoo, suspension

Pert Plus for Men Daily Dandruff by

Drug Labeling and Warnings

Pert Plus for Men Daily Dandruff by is a Otc medication manufactured, distributed, or labeled by Idelle Labs, Ltd, Body Blue 2006 Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Pert Plus for Men Daily Dandruff

Pert Plus for Men Daily Dandruff 2 in 1 Shampoo Plus Conditioner

controls dandruff with pyrithione zinc

with strengthening ingredients

MM1

Active Ingredient

Zinc Pyrithione 1.0%

Purpose:

Anti-Dandruff

Uses

Controls the symptoms of dandruff.

Warning:

For external use only

When using this product

avoid contact with eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor

if condition worsens or does not improve after regular use of this product as directed.

Keep this and all drugs out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions:

For best results, use at least twice a week or as directed by a doctor. Gently massage into wet hair, lather and rinse. Repeat if desired.

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.

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

label

INGREDIENTS AND APPEARANCE

PERT PLUS FOR MEN DAILY DANDRUFF 
pyrithione zinc shampoo, suspension

Product 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