HEAD AND SHOULDERS CLINICAL ITCH RELIEF SCALP MIST- pyrithione zinc liquid 
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 ® Clinical Itch Relief Scalp Mist

Drug Facts

Active ingredient

Pyrithione zinc 0.1%

Purpose

Anti-dandruff

Use

for the relief of 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, niacinamide, PEG-40 hydrogenated castor oil, phenoxyethanol, caffeine, bis-PEG/PPG-16/16 PEG/PPG-16/16 dimethicone, glycerin, benzyl alcohol, fragrance, menthol, acrylates/C10-30 alkyl acrylate crosspolymer, panthenol, tetrahydroxypropyl ethylenediamine, ethylhexylglycerin, mentha piperita (peppermint) oil, mentha arvensis leaf oil.

Questions (or comments)?

1-800-723-9569

Dist. by PROCTER & GAMBLE,
CINCINNATI, OH 45202

PRINCIPAL DISPLAY PANEL - 125 mL bottle label

head &
shoulders ®
pyrithione zinc dandruff treatment

CLINICAL

ITCH RELIEF

SCALP MIST

SOOTHES DANDRUFF ITCH

USE BETWEEN WASHES

WITH INTENSE

COOLING MENTHOL

4.2 FL OZ (125 mL)

HS

HEAD AND SHOULDERS CLINICAL ITCH RELIEF SCALP MIST 
pyrithione zinc liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69423-529
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (UNII: R953O2RHZ5) (PYRITHIONE ZINC - UNII:R953O2RHZ5) PYRITHIONE ZINC0.1 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERIN (UNII: PDC6A3C0OX)  
MENTHA ARVENSIS LEAF OIL (UNII: 1AEY1M553N)  
WATER (UNII: 059QF0KO0R)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)  
NIACINAMIDE (UNII: 25X51I8RD4)  
PANTHENOL (UNII: WV9CM0O67Z)  
CAFFEINE (UNII: 3G6A5W338E)  
BIS-PEG/PPG-16/16 PEG/PPG-16/16 DIMETHICONE (UNII: 55A74AJ3KB)  
MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
EDETOL (UNII: Q4R969U9FR)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
CARBOMER INTERPOLYMER TYPE A (55000 CPS) (UNII: 59TL3WG5CO)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69423-529-12125 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product11/17/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalM03211/17/2020
Labeler - The Procter & Gamble Manufacturing Company (004238200)

Revised: 1/2023
Document Id: ec092c92-70fd-665f-e053-2a95a90afdd0
Set id: b6aec5b7-b278-4248-e053-2995a90aa9c9
Version: 2
Effective Time: 20230127
 
The Procter & Gamble Manufacturing Company