DZUL ANTI-DANDRUFF CONDITIONER- pyrithione zinc cream

DZUL ANTI-DANDRUFF CONDITIONER by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENT

Pyrithione Zinc 2%

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

When using this product do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

STOP USE

Stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

KEEP OUT OF REACH OF CHILDREN

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

DOSAGE & ADMINISTRATION

Apply a small amount quantity of the product into hair and massage the scalp.
Allow the product to act for 5 minutes.
Rinse thoroughly with enough water.

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), Cetearyl Alcohol, Stearyl Alcohol, Cetyl Alcohol, Caprylic/Capric Triglyceride, Behentrimonium Methosulfate, Caprylyl Glycol, Fragrance (Parfum), Organic Butyrospermum Parkii (Shea) Butter, Panthenol, Hydrolyzed Keratin, Guar Hydroxypropyltrimonium Chloride, Ricinus Communis (Castor) Seed Oil, Disodium EDTA, Propylene Glycol, Biotin, Argania Spinosa Kernel Oil, Malus Domestica Fruit Cell Culture Extract, Xanthan Gum, Sodium Benzoate, Glycerin, Algae Extract, Citric Acid, Phenoxyethanol, Chlorophenesin, Cetrimonium Chloride, Limonene, Linalool.

QUESTIONS

Questions or comments?

Call (305)-900-8256

DZUL ANTI-DANDRUFF CONDITIONER

INGREDIENTS AND APPEARANCE

DZUL ANTI-DANDRUFF CONDITIONER 
pyrithione zinc cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 83037-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5)	PYRITHIONE ZINC	2 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
ARGANIA SPINOSA WHOLE (UNII: 83K6O4FR76)
XANTHAN GUM (UNII: TTV12P4NEE)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
PANTHENOL (UNII: WV9CM0O67Z)
BIOTIN (UNII: 6SO6U10H04)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
MALUS DOMESTICA WHOLE (UNII: 04W636S1V3)
EDETATE DISODIUM (UNII: 7FLD91C86K)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
LIMONENE, (+)- (UNII: GFD7C86Q1W)
ASCOPHYLLUM NODOSUM (UNII: 168S4EO8YJ)
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)
CASTOR OIL (UNII: D5340Y2I9G)
GLYCERIN (UNII: PDC6A3C0OX)
CHLORPHENESIN (UNII: I670DAL4SZ)
CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)
CETYL ALCOHOL (UNII: 936JST6JCN)
SHEA BUTTER (UNII: K49155WL9Y)
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)
MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)
BEHENTRIMONIUM METHOSULFATE (UNII: 5SHP745C61)
LINALOOL, (+/-)- (UNII: D81QY6I88E)

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 83037-002-08	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 Drug	M032	09/22/2023

Labeler - Caball Sales, Inc. (047422138)