Medication Guide App

Dandruff Shampoo

Dosage form: lotion/shampoo
Ingredients: PYRITHIONE ZINC 1kg in 100L
Labeler: Cardinal Health
NDC Code: 37205-311

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                      Purpose

Pyrithione Zinc   1%                          Anti-Dandruff

Use  helps prevent recurrence of flaking and itching associated with 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 ask a doctor if
• condition worsens or does not improve after regular use as directed

Keep out of reach of children.  If swallowed, get medical help or contact a Poison Control Center right away.

Directions
• shake well • for maximum dandruff control, use every time you shampoo • wet hair, message onto scalp, rinse, repeat if desired
• for best result use at least twice a week or as directed by doctor

Inactive ingredients water, sodium laureth sulfate, glycol distearate, sodium lauryl sulfate, cocamidopropyl betaine, cocamide MEA,
zinc carbonate, behentrimonium chloride, fragrance, magnesium sulfate, sodium benzoate, zinc chloride, sodium citrate, benzyl alcohol, sodium chloride, sodium hydroxide, blue 1, red 4

Compare to
Head + Shoulders
active ingredient
Pyrithione Zinc
Dandruff
Shampoo
Everyday Clean
Everyday basi cleaning
for Normal or Oily Hair
14.2 FL OZ
(420 mL)

DANDRUFF SHAMPOO 
pyrithione zinc lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37205-311
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC1 kg  in 100 L
Inactive Ingredients
Ingredient NameStrength
SODIUM LAURETH SULFATE 
GLYCOL DISTEARATE 
SODIUM LAURYL SULFATE 
COCAMIDOPROPYL BETAINE 
ZINC CARBONATE 
BEHENTRIMONIUM CHLORIDE 
SODIUM BENZOATE 
ZINC 
SODIUM CITRATE 
BENZYL ALCOHOL 
SODIUM CHLORIDE 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:37205-311-15.42 L in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart35805/19/1998
Labeler - Cardinal Health (097537435)
Registrant - Vi Jon (790752542)
Establishment
NameAddressID/FEIOperations
Vi Jon790752542manufacture

Revised: 07/2010
 
Cardinal Health

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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