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Sulfur 8 Five Star Anti-Dandruff Hair Groom

Medically reviewed on January 19, 2018

Dosage form: cream
Ingredients: PYRITHIONE ZINC 1mg in 1g
Labeler: J. Strickland & Co.
NDC Code: 12022-030

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.

Sulfur 8 Five Star Anti-Dandruff Hair Groom Cream

Active Ingredients

Pyrithione Zinc, 0.1%

Purpose

Anti-dandruff

Use:

Controls scalp itching and flaking due to dandruff

Warnings:

For external use only

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

Stop use and consult a doctor if 
  • condition worsens or does not improve after regular use.

Keep out of reach of children

If swallowed, get medical helpor call a poison contril center at once.

Directions
  • Apply to the affected area 1-4 times daily, or as dircted by a doctor.

Inactive Ingredients

Water, Petrolatum, Mineral Oil, Glycerin, Ricinis Communis (Castor) Seed Oil, Stearyl Alcohol, Behentrimonium Methosulfate, Beeswax (Cera Alba), Dimethicone, Lanolin, Oleth-20, Polyquaterinium-11, Allantoin, Panthenol, Propylene Glycol, Butylene Glycol, Cetyl Alcohol, Sorbitan Trioleate, Diazolidinyl Urea, Methylparaben, Sodium Sulfate, Propylparaben, Fragrance (Parfum). 

Package Labeling

SULFUR 8 FIVE STAR ANTI-DANDRUFF HAIR GROOM 
pyrithione zinc cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-030
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC1 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
WATER 
PETROLATUM 
MINERAL OIL 
GLYCERIN 
STEARYL ALCOHOL 
BEHENTRIMONIUM METHOSULFATE 
DIMETHICONE 
LANOLIN 
OLETH-20 
ALLANTOIN 
PANTHENOL 
PROPYLENE GLYCOL 
BUTYLENE GLYCOL 
CETYL ALCOHOL 
SORBITAN TRIOLEATE 
DIAZOLIDINYL UREA 
METHYLPARABEN 
SODIUM SULFATE 
PROPYLPARABEN 
Packaging
#Item CodePackage Description
1NDC:12022-030-0099 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H04/29/2010
Labeler - J. Strickland & Co. (007023112)
Registrant - J. Strickland & Co. (007023112)
Establishment
NameAddressID/FEIOperations
J. Strickland & Co.007023112manufacture(12022-030), pack(12022-030), label(12022-030)

 
J. Strickland & Co.

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.

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