HEAD AND SHOULDERS INSTANT OIL CONTROL- pyrithione zinc lotion/shampoo 
The Procter & Gamble Manufacturing Company

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 and Shoulders ®

Instant Oil Control

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 laureth sulfate, cocamideMEA, sodium xylenesulfonate, zinc carbonate, glycol distearate, sodium lauryl sulfate, cocamidopropyl betaine, fragrance, sodiumchloride, dimethicone, menthol, guar hydroxypropyltrimonium chloride, sodium benzoate, stearyl alcohol,magnesiumcarbonate hydroxide, cetyl alcohol, polyquaternium-76, citrus limon (lemon) fruit extract,methylchloroisothiazolinone, methylisothiazolinone, eucalyptol, camphor, yellow5, blue 1.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 380 mL Bottle Label

head &
shoulders
®

pyrithione zinc dandruff shampoo

INSTANT
oil control

DAILY SHAMPOO

controls hair and scalp oils

FLAKE FREE.*
UP TO 100%
GUARANTEED^

infused with mango & citrus essence

12.8 FL OZ (380 mL)

HS

HEAD AND SHOULDERS  INSTANT OIL CONTROL
pyrithione zinc lotion/shampoo
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-344
Route of Administration TOPICAL
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC 1 g  in 100 mL
Inactive Ingredients
Ingredient Name Strength
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE) (UNII: B16G315W7A)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
EUCALYPTOL (UNII: RV6J6604TK)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
COCO MONOETHANOLAMIDE (UNII: C80684146D)  
ZINC CARBONATE (UNII: EQR32Y7H0M)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
CETYL ALCOHOL (UNII: 936JST6JCN)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
MAGNESIUM CARBONATE HYDROXIDE (UNII: YQO029V1L4)  
STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
LEMON (UNII: 24RS0A988O)  
METHYLCHLOROISOTHIAZOLINONE (UNII: DEL7T5QRPN)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:37000-344-38 380 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2014
2 NDC:37000-344-66 665 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product 09/01/2014 02/20/2018
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 09/01/2014
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2018
Document Id: 7c264f18-053e-ae11-e053-2a91aa0aa34c
Set id: 83f0f5e0-2883-4c68-a6bc-f22f6c9d9f80
Version: 4
Effective Time: 20181203
 
The Procter & Gamble Manufacturing Company