Skip to Content

Head and Shoulders Men Refresh

Medically reviewed on October 21, 2016

Dosage form: lotion/shampoo
Ingredients: PYRITHIONE ZINC 1g in 100mL
Labeler: Procter & Gamble Manufacturing Company
NDC Code: 37000-096

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.

Head and Shoulders ®

Men Refresh

Drug Facts

Active ingredient

Pyrithione zinc 1%

Purpose

Anti-dandruff

Uses

helps prevent recurrence of flaking and itching associated with dandruff.

Warnings

For external use only.

When using this product

  • avoid contact with 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 of this product as directed.

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

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

Inactive ingredients

Water, sodium lauryl sulfate, sodium laureth sulfate, glycol distearate, zinc carbonate, sodium chloride, fragrance, sodium xylenesulfonate, cocamidopropyl betaine, dimethicone, sodium benzoate, guar hydroxypropyltrimonium chloride, magnesium carbonate hydroxide, methylchloroisothiazolinone, methylisothiazolinone, blue 1, red 33.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 400 mL Bottle Label

3 Action

FORMULA

head &

shoulders ®

pyrithione zinc dandruff shampoo

MEN

refresh

cools and energizes scalp

FLAKE FREE.*

UP TO 100%

GUARANTEED^

13.5 FL OZ (400 mL)

HEAD AND SHOULDERS  MEN REFRESH
pyrithione zinc lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-096
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURYL SULFATE 
SODIUM LAURETH-3 SULFATE 
GLYCOL DISTEARATE 
ZINC CARBONATE 
SODIUM CHLORIDE 
SODIUM XYLENESULFONATE 
COCAMIDOPROPYL BETAINE 
DIMETHICONE 
SODIUM BENZOATE 
MAGNESIUM CARBONATE HYDROXIDE 
METHYLCHLOROISOTHIAZOLINONE 
METHYLISOTHIAZOLINONE 
FD&C BLUE NO. 1 
D&C RED NO. 33 
Packaging
#Item CodePackage Description
1NDC:37000-096-70700 mL in 1 BOTTLE, PLASTIC
2NDC:37000-096-40400 mL in 1 BOTTLE, PLASTIC
3NDC:37000-096-95950 mL in 1 BOTTLE, PUMP
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H09/01/2013
Labeler - Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
Arch Chemicals, Inc.002220804api manufacture(37000-096)

 
Procter & Gamble Manufacturing Company

Further information

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

Hide