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Sulfur 8 Fresh Anti-Dandruff Oil Moisturizing

Medically reviewed on January 19, 2018

Dosage form: lotion
Ingredients: PYRITHIONE ZINC 1mg in 1mL
Labeler: J. Strickland & Co.
NDC Code: 12022-029

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 Fresh Anti-Dandruff Oil Moisturizing Lotion

Active Ingredients

Pyrithione Zinc, 0.1%

Purpose

Antidandruff

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 help or call a poison control center at once.

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

Inactive Ingredients

water, Mineral Oil, Aloe Barbadensis Leaf Juice, Isopropyl Myristate, Stearyl Alcohol, Ceteareth-20, Sodium Carbomer, Simmondsia Chinensis (Jojoba) Seed Oil, Hydrolyzed Collagen, Propylene Glycol, Tocopheryl Acetate, Methylparaben, Propylparaben, Diazolidinyl Urea, Sodium Lauryl Sulfate, Panthenol, Fragrance.

Package Labeling

SULFUR 8 FRESH ANTI-DANDRUFF OIL MOISTURIZING 
pyrithione zinc lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:12022-029
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
MINERAL OIL 
ALOE VERA LEAF 
ISOPROPYL MYRISTATE 
STEARYL ALCOHOL 
POLYOXYL 20 CETOSTEARYL ETHER 
JOJOBA OIL 
PROPYLENE GLYCOL 
.ALPHA.-TOCOPHEROL ACETATE 
METHYLPARABEN 
PROPYLPARABEN 
DIAZOLIDINYL UREA 
SODIUM LAURYL SULFATE 
PANTHENOL 
Packaging
#Item CodePackage Description
1NDC:12022-029-00355 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H02/06/2008
Labeler - J. Strickland & Co. (007023112)
Registrant - J. Strickland & Co. (007023112)
Establishment
NameAddressID/FEIOperations
J. Strickland & Co.007023112manufacture(12022-029), pack(12022-029), label(12022-029)

 
J. Strickland & Co.

Further information

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

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