HEAD AND SHOULDERS  OCEAN LIFT- pyrithione zinc lotion/shampoo 
Procter & Gamble Manufacturing Co.

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.

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Head & Shoulders® Shampoo
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

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, sea salt, 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

head &
shoulders®

pyrithione zinc
dandruff shampoo

IMPROVES HAIR & SCALP
HEALTH GUARANTEED

ocean lift

with sea mineral essence,
invigorates hair and scalp

23.7 FL OZ
(700 mL)

99842192

Principal Display Panel - 700 mL Bottle Label
HEAD AND SHOULDERS   OCEAN LIFT
pyrithione zinc lotion/shampoo
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-788
Route of Administration TOPICAL DEA Schedule     
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Pyrithione Zinc (UNII: R953O2RHZ5) (Pyrithione Zinc - UNII:R953O2RHZ5) Pyrithione Zinc 1 g  in 1 mL
Inactive Ingredients
Ingredient Name Strength
water (UNII: 059QF0KO0R)  
sodium lauryl sulfate (UNII: 368GB5141J)  
sodium laureth-3 sulfate (UNII: BPV390UAP0)  
glycol distearate (UNII: 13W7MDN21W)  
zinc carbonate (UNII: EQR32Y7H0M)  
sodium chloride (UNII: 451W47IQ8X)  
sodium xylenesulfonate (UNII: G4LZF950UR)  
cocamidopropyl betaine (UNII: 5OCF3O11KX)  
dimethicone (UNII: 92RU3N3Y1O)  
sodium benzoate (UNII: OJ245FE5EU)  
magnesium carbonate hydroxide (UNII: YQO029V1L4)  
sea salt (UNII: 87GE52P74G)  
methylchloroisothiazolinone (UNII: DEL7T5QRPN)  
methylisothiazolinone (UNII: 229D0E1QFA)  
fd&c blue no. 1 (UNII: H3R47K3TBD)  
fd&c yellow no. 5 (UNII: I753WB2F1M)  
Product Characteristics
Color TURQUOISE Score     
Shape Size
Flavor Imprint Code
Contains     
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37000-788-14 420 mL in 1 BOTTLE, PLASTIC
2 NDC:37000-788-23 700 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC MONOGRAPH FINAL part358H 01/01/2006 01/19/2016
Labeler - Procter & Gamble Manufacturing Co. (004238200)

Revised: 6/2014
Document Id: be4deab7-ed55-43a9-bbe9-43ed9af4bca9
Set id: 64a62348-610d-4043-ad43-b3b00d8b92a5
Version: 3
Effective Time: 20140620
 
Procter & Gamble Manufacturing Co.