FDA Label for Australian Gold Defense Zone Anti-dandruff Leave-in Treatment
View Indications, Usage & Precautions
Australian Gold Defense Zone Anti-dandruff Leave-in Treatment Product Label
The following document was submitted to the FDA by the labeler of this product Prime Enterprises, Inc.. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.
Principal Display Panel - 118 Ml Bottle Label
Defense
Zone
Medicated
LEAVE-IN
TREATMENT
Anti-Dandruff
Step
3
Relieves Dryness
Locks in Moisture
4 FL OZ (118mL)
Active Ingredient:
Pyrithione Zinc 0.22%
Purpose
Antidanruff
Indications:
- Controls the symptoms of dandruff.
- Helps prevent recurrence of scalp itching and flaking associated with dandruff.
Warning:
Otc - When Using
When using this product
- Avoid contact with the eyes. If contact occurs, rinse eyes thorougly with water.
Otc - Stop Use
Stop use and ask a doctor
- If condition worsens or does not improve after regular use of this product as directed.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
- If swallowed, get medical help or contact a Poison Control Center right away
Directions:
- Shake well.
- Use after shampooing and towel drying hair. Part hair section by section. Apply directly onto the scalp and spread using fingertips. Gently massage into scalp. Leave in.
- Apply to affected areas one to four times daily or as directed by a doctor
- Children under 6 months of age: ask a doctor.
Inactive Ingrediets:
Caprylyl Glycol, Ceteareth-20, Cetearyl Alcohol, Cetrimonium Bromide, Cetyl Alcohol, Chlorphenesin, Citric Acid, Disodium EDTA, Elaeis Guineensis (Palm) Oil, Fragrance, Glycerin, Phenoxyethanol, Sodium Hydroxide, Stearyl Dihydroxypropyldisodium Oligosaccharides, Water
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