CRAWFORD DANDRUFF- pyrithione zinc shampoo

Crawford Dandruff by

Drug Labeling and Warnings

Crawford Dandruff by is a Otc medication manufactured, distributed, or labeled by Keefe Group. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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Drug Facts

ACTIVE INGREDIENT

Active Ingredient

Pyrithione zinc 0.5%

PURPOSE

Purpose

Anti dandruff

INDICATIONS & USAGE

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

WARNINGS

Warnings using this product
For external use only.

Keep this and all drugs out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

Directions: For maximum dandruff control, use at least twice a week. Wet hair, massage through hair and scalp, rinse and repeat if desired.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS:

Water (Aqua), Sodium Laureth Sulfate, Sodium Chloride, Glycol Distearate, Cocamidopropyl Betaine, Polyquaternium-7, Fragrance, Tetrasodium EDTA, Methylchloroisothiazolinone, Methylisothiazolinone, FD&C Blue #1

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Manufactured for

Crawford Supply St. Louis, MO 63132

PRODUCT OF CANADA

PRINCIPAL DISPLAY PANEL

Crawford

Dandruff Shampoo

Clears Hair of Dandruff Flakes

4 fl. oz. (118 mL)

INGREDIENTS AND APPEARANCE

CRAWFORD DANDRUFF 
pyrithione zinc shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 51870-005
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	0.5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
SODIUM LAURETH SULFATE (UNII: BPV390UAP0)
GLYCOL DISTEARATE (UNII: 13W7MDN21W)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
EDETATE SODIUM (UNII: MP1J8420LU)
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 51870-005-04	118 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/01/2012
2	NDC: 51870-005-12	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	10/24/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358H	10/01/2012

Labeler - Keefe Group (839439601)