WECARE ANTI-DANDRUFF- antidandruff shampoo liquid

WeCare Anti-Dandruff by

Drug Labeling and Warnings

WeCare Anti-Dandruff by is a Otc medication manufactured, distributed, or labeled by Dynarex Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Pyrithione Zinc 0.5%

Purpose

Anti-Dandruff

Use

Helps eliminate irritation and flaking associated with dandruff

Warnings

For External Use Only

When using this product

• Avoid contact with eyes
• If contact occurs, rinse eyes with plenty of water

Stop use and ask a doctor if

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

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

Directions

• wet hair
• lather
• massage onto scalp
• rinse well
• repeat if desired
• for best results, use regularly

Inactive ingredients

Water, Sodium Laureth Sulfate, Cocamide MEA, Cocamidopropyl Betaine, Sodium Chloride, Glycol Distearate, Acrylates Copolymer, Coco-Glucoside, Styrene/Acrylates Copolymer, Dimethiconol, Glyceryl Oleate, Polyquaternium-10, Citric Acid, TEA-dodecyl-benzene-sulfonate, Sodium Hydroxide, Benzyl Alcohol, Sodium Benzoate, Methylchloroisothiazolinone, Methylisothiazolinone, Amyl Cinnamal, Benzyl Salicylate, CI42090

1398 Label

INGREDIENTS AND APPEARANCE

WECARE ANTI-DANDRUFF 
antidandruff shampoo liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 67777-139
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	5 g  in 1000 g

Inactive Ingredients
Ingredient Name	Strength
SODIUM CHLORIDE (UNII: 451W47IQ8X)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
.ALPHA.-AMYLCINNAMALDEHYDE (UNII: WC51CA3418)
WATER (UNII: 059QF0KO0R)
STYRENE/ACRYLAMIDE COPOLYMER (MW 500000) (UNII: 5Z4DPO246A)
DIMETHICONOL (2000 CST) (UNII: T74O12AN6Y)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
SODIUM BENZOATE (UNII: OJ245FE5EU)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
GLYCERYL MONOOLEATE (UNII: C4YAD5F5G6)
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) (UNII: GMR4PEN8PK)
TRIETHANOLAMINE DODECYLBENZENESULFONATE (UNII: 8HM7ZD48HN)
BENZYL ALCOHOL (UNII: LKG8494WBH)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
BUTYL ACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID COPOLYMER (18000 MW) (UNII: JZ1374NL9E)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
COCO MONOETHANOLAMIDE (UNII: C80684146D)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
COCO GLUCOSIDE (UNII: ICS790225B)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 67777-139-80	12 in 1 CASE	10/11/2018
1		335 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/11/2018

Labeler - Dynarex Corporation (008124539)