HEAD AND SHOULDERS CLINICAL STRENGTH DANDRUFF DEFENSE SENSITIVE SCALP- selenium sulfide lotion/shampoo 
The Procter & Gamble Manufacturing Company

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Head and Shoulders ®

Clinical Strength Dandruff Defense Sensitive Scalp Shampoo

Drug Facts

Active ingredient

Selenium Sulfide 1%

Purpose

Anti-dandruff, anti-seborrheic dermatitis

Uses

helps prevent recurrence of flaking, itching, irritation, scaling and redness associated with dandruff and seborrheic dermatitis.

Warnings

For external use only.

Ask a doctor before use if you have a condition that covers a large area of the body.

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, glycol distearate, sodiumchloride, cocamidopropyl betaine, sodiumcitrate, sodium xylenesulfonate, dimethicone, fragrance, citric acid, sodium benzoate, tetrasodium EDTA, hydroxypropyl methylcellulose, aloe barbadensis leaf juice

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - BOTTLE LABEL

head &

shoulders ®

selenium sulfide dandruff &

seborrheic dermatitis shampoo

Clinical Strength

Dandruff Defense

Sensitive

Scalp

13.5 FL OZ (400 mL)

HS

HEAD AND SHOULDERS CLINICAL STRENGTH DANDRUFF DEFENSE SENSITIVE SCALP 
selenium sulfide lotion/shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-642
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SELENIUM SULFIDE (UNII: Z69D9E381Q) (SELENIUM SULFIDE - UNII:Z69D9E381Q) SELENIUM SULFIDE1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
EDETATE SODIUM (UNII: MP1J8420LU)  
WATER (UNII: 059QF0KO0R)  
SODIUM LAURYL SULFATE (UNII: 368GB5141J)  
GLYCOL DISTEARATE (UNII: 13W7MDN21W)  
SODIUM CHLORIDE (UNII: 451W47IQ8X)  
SODIUM XYLENESULFONATE (UNII: G4LZF950UR)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-642-40400 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/22/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03204/22/2022
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 12/2023
Document Id: 0c929c77-c696-a582-e063-6394a90aeab1
Set id: eedc5e57-8047-eab7-e053-2a95a90a2e2a
Version: 2
Effective Time: 20231215
 
The Procter & Gamble Manufacturing Company