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Sulfur 8 Aqua Blue

Medically reviewed on January 19, 2018

Dosage form: shampoo, suspension
Ingredients: PYRITHIONE ZINC 10mg in 1mL
Labeler: J. Strickland & Co.
NDC Code: 12022-024

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 Aqua Blue Shampoo

Active Ingredients

Pyrithione Zinc, 1%

Purpose

Antidandruff

Use:

relieves scalp itching, irritation, redness, scaling and flaking associated with dandruff

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 into eyes. If contact occurs, rinse eyes thoroughly with water.

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

Keep out of reach of children

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

Directions
  • shake well
  • for best results, use twice a week 
  • wet hair, apply shampoo, lather, rinse & repeat

Inactive Ingredients

SD Alcohol 40, Water, Propylene Glycol, Benzyl Alcohol, Menthol.

Package Labeling

SULFUR 8 AQUA BLUE 
pyrithione zinc shampoo, suspension
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-024
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
AMMONIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
HYPROMELLOSE, UNSPECIFIED 
GLYCOL STEARATE 
MAGNESIUM ALUMINUM SILICATE 
BENZYL ALCOHOL 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
TRIETHYLENE GLYCOL 
MAGNESIUM NITRATE 
MAGNESIUM CHLORIDE 
CITRIC ACID MONOHYDRATE 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:12022-024-00222 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H07/15/2002
Labeler - J. Strickland & Co. (007023112)
Registrant - J. Strickland & Co. (007023112)
Establishment
NameAddressID/FEIOperations
J. Strickland & Co.007023112manufacture(12022-024), pack(12022-024), label(12022-024)

 
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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