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Australian Gold Metro 365 Medicated 2 in 1 Anti-Dandruff

Dosage form: shampoo
Ingredients: PYRITHIONE ZINC 10.32mg in 1mL
Labeler: Prime Enterprises Inc.
NDC Code: 58443-0242

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Australian Gold Metro 365 Medicated 2 in 1 Anti - Dandruff

Active Ingredients

Pyrithione Zinc 1%

Purpose

Antidandruff

Indications
  • Controls the symptoms of dandruff.
  • Helps prevent recurrence of scalp itching and flaking associated with antidandruff.

Warnings

For external use only.

When using this product
  • Avoid contact with the eyes. If contact occurs, rinse eyes thouroughly with water.

Stop use and ask a doctor
  • If condition 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 a Poison Control Center right away.

Directions
  • Shake well
  • Wet hair, lather and massage into scalp, rinse hair thoroughly, repeat if desired.
  • For best results use at least twice a week or as directed by a doctor.
  • Children under 6 months of age: ask a doctor.

Acrylates Copolymer, Caprylyl Glycol, Chlorphenesin, Cocamide MEA, Cocamidopropyl Betaine, Dimethicone, Disodium EDTA, Fragrance, Glycol Stearate, Phenoxyethanol, Propylene Glycol, Sodium Hydroxide, Sodium Laureth Sulfate, Stearyl Dihydroxypropyldimonium Oligosaccharides, Water

Other Information
  • Protect from heat.

Questions or Comments?

Call toll free 1-855-548-4653

Australian Gold Metro 365 Medicated 2 in 1 Anti-Dandruff

AUSTRALIAN GOLD  METRO 365 MEDICATED 2 IN 1 ANTI-DANDRUFF
pyrithione zinc 1% shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:58443-0242
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC10.32 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
CHLORPHENESIN 
COCAMIDOPROPYL BETAINE 
DIMETHICONE 
EDETATE DISODIUM 
GLYCOL STEARATE 
PHENOXYETHANOL 
SODIUM HYDROXIDE 
SODIUM LAURETH SULFATE 
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) 
CAPRYLYL GLYCOL 
WATER 
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) 
COCO MONOETHANOLAMIDE 
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage Description
1NDC:58443-0242-5266 mL in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H10/07/2016
Labeler - Prime Enterprises Inc. (101946028)
Registrant - Prime Enterprises Inc. (101946028)
Establishment
NameAddressID/FEIOperations
Prime Enterprises Inc.101946028manufacture(58443-0242), label(58443-0242), analysis(58443-0242), pack(58443-0242)

 
Prime Enterprises Inc.

Medically reviewed on Oct 8, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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