DZUL ANTI-DANDRUFF- zinc pyrithione shampoo

DZUL ANTI-DANDRUFF by

Drug Labeling and Warnings

DZUL ANTI-DANDRUFF by is a Otc medication manufactured, distributed, or labeled by Caball Sales, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Zinc Pyrithione 1%

PURPOSE

Anti-Dandruff

INDICATIONS & USAGE

For the relief of the symptoms of dandruff.

WARNINGS

For external use only.

Do not use on wounds or damaged skin or on a child under 12 years of age unless directed by a physician.

WHEN USING

Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

STOP USE

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

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Apply a small amount quantity of the product into hair and massage the scalp.
Rinse thoroughly with enough water, repeat if needed.

For best results, use at least twice a week or as directed by a doctor.

OTHER SAFETY INFORMATION

See on the bottom of the bottle for lot number and expiration date.

INACTIVE INGREDIENT

Water (Aqua), Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Betaine, Acrylates Copolymer, Cocamide MEA, Cocamidopropylamine Oxide, Caprylyl Glycol, Hexylene Glycol, Fragrance (Parfum), Polyquaternium-7, Sodium Hydroxide, Disodium EDTA, Citric Acid, Panthenol, Phenoxyethanol, FD&C Blue No.1 (CI 42090), Hexyl Cinnamal, Benzyl Salicylate, Coumarin, Alpha-Isomethyl Ionone, Geraniol, Linalool.

QUESTIONS

QUESTION OR COMMENTS?

Call (305)-900-8256

DZUL ANTI-DANDRUFF SHAMPOO

INGREDIENTS AND APPEARANCE

DZUL ANTI-DANDRUFF 
zinc pyrithione shampoo

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83037-001
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 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
COCO MONOETHANOLAMIDE (UNII: C80684146D)
.ALPHA.-HEXYLCINNAMALDEHYDE (UNII: 7X6O37OK2I)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
SODIUM HYDROXIDE (UNII: 55X04QC32I)
WATER (UNII: 059QF0KO0R)
SODIUM C14-16 OLEFIN SULFONATE (UNII: O9W3D3YF5U)
COCAMIDOPROPYLAMINE OXIDE (UNII: M4SL82J7HK)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
LINALOOL, (+)- (UNII: F4VNO44C09)
BENZYL SALICYLATE (UNII: WAO5MNK9TU)
COUMARIN (UNII: A4VZ22K1WT)
PANTHENOL (UNII: WV9CM0O67Z)
GERANIOL (UNII: L837108USY)
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
EDETATE DISODIUM (UNII: 7FLD91C86K)
POLYQUATERNIUM-7 (70/30 ACRYLAMIDE/DADMAC; 1600 KD) (UNII: 0L414VCS5Y)
ISOMETHYL-.ALPHA.-IONONE (UNII: 9XP4LC555B)
HEXYLENE GLYCOL (UNII: KEH0A3F75J)

Product Characteristics
Color	blue	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83037-001-08	236 mL in 1 BOTTLE; Type 0: Not a Combination Product	09/22/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	M032	09/22/2023

Labeler - Caball Sales, Inc. (047422138)