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Head Remedy Dandruff Conditioner

Dosage form: emulsion
Ingredients: PYRITHIONE ZINC 1.0g in 100g
Labeler: KPSS, Inc.
NDC Code: 25237-0516

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.

Drug Facts

Active Ingredient: Zinc Pyrithione 1.0%

Purpose: Antidandruff

Use: Controls dandruff and flaking for a healthy scalp.

Warnings: For external use only.

Ask a doctor before use if you have: seborrheic dermatitis that covers a large area of the body.

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

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

Keep Out of Children's Reach: If swallowed, get medical help or contact a Poison Control Center right away.

Directions: Apply small amount on shampooed hair. Massage into wet hair and scalp. Leave in 2 minutes and rinse. For best results, use at least 2 times a week.

Distributed by KPSS Inc., Linthicum Heights, MD 21090 USA, 1-800-342-5567

MM1: 8oz_dandruff_conditioner_label.jpg

water, cetearyl alcohol, isopropyl palmitate, stearamidopropyl dimethylamine, phenethyl dimethicone, mineral oil, lactic acid, panthenol, butylene glycol, propylene glycol, glucose, Foeniculum vulgare (Fennel) fruit extract, Melissa officinalis (Balm) extract, Salvia officinalis (Sage) extract, Rosmarinus officinalis (Rosemary) extract, Urtica dioica (Nettle) extract, Equisetum arvense (Horsetail) extract, Humulus lupulus (Hops) extract, Chamomilla recutita (Matricaria) flower extract, caramel, sorbitol, sodium benzoate, potassium sorbate, DMDM Hydantoin, phenoxyethanol, tartaric acid, methylparaben, propylparaben, isobutylparaben, ethylparaben, butylparaben, fragrance, blue 1

pyrithione zinc emulsion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:25237-0516
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
#Item CodePackage Description
1NDC:25237-0516-1249.4 g in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H01/01/2006
Labeler - KPSS, Inc. (808543149)

Revised: 08/2010
KPSS, Inc.

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.