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Head and Shoulders Ocean Lift

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

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 ®

Ocean Lift

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, yellow 5.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 700 mL Bottle Label

3 Action

FORMULA

head &

shoulders ®


pyrithione zinc dandruff shampoo

ocean lift

for an invigorating scent


FLAKE FREE.*

UP TO 100%

GUARANTEED^

23.7 FL OZ

(700 mL)

HEAD AND SHOULDERS  OCEAN LIFT
pyrithione zinc lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:37000-100
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 
FD&C YELLOW NO. 5 
Packaging
#Item CodePackage Description
1NDC:37000-100-70700 mL in 1 BOTTLE, PLASTIC
2NDC:37000-100-40400 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H09/01/201309/06/2019
Labeler - The Procter & Gamble Manufacturing Company (004238200)
Establishment
NameAddressID/FEIOperations
Arch Chemicals, Inc.002220804api manufacture(37000-100)

 
The Procter & Gamble Manufacturing Company

Medically reviewed on Dec 14, 2017

Further information

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

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