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Kiehls Since 1851 Scalp Purifying Dandruff

Dosage form: shampoo
Ingredients: PYRITHIONE ZINC 10mg in 1mL
Labeler: L'Oreal USA Products Inc
NDC code: 49967-799

Medically reviewed by Drugs.com. Last updated on Dec 25, 2023.

Drug Facts

Active ingredient

Pyrithione zinc 1%

Purpose

Antidandruff

Uses
  • controls the symptoms of dandruff
  • reduces recurrence of the symptoms of dandruff
  • for the relief of scalp itching, irritation and flaking associated with dandruff

Warnings

For external use only

When using this product

avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a physician if

condition worsens or does not improve after regular use

Keep 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 physican
  • shake well
  • wet hair and apply a small amount of shampoo
  • massage vigorously
  • rinse well

Inactive ingredients

water, sodium laureth sulfate, disodium cocoamphodiacetate, sodium chloride, glycol disearate, PPG-5-ceteth-20, sodium benzoate, carbomer, polyquaternium-10, salicylic acid, methol, citric acid, rosmarinus officinalis (rosemary) leaf oil, thymus mastichina flower oil, linalool, aloe barbadensis leaf juice, sodium hydroxide

KIEHLS SINCE 1851 SCALP PURIFYING DANDRUFF 
pyrithione zinc shampoo
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-799
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC10 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER 
SODIUM LAURETH SULFATE 
DISODIUM COCOAMPHODIACETATE 
SODIUM CHLORIDE 
GLYCOL DISTEARATE 
PPG-5-CETETH-20 
SODIUM BENZOATE 
CARBOXYPOLYMETHYLENE 
POLYQUATERNIUM-10 (1000 MPA.S AT 2%) 
SALICYLIC ACID 
MENTHOL 
CITRIC ACID MONOHYDRATE 
ROSEMARY OIL 
THYMUS MASTICHINA FLOWERING TOP OIL 
LINALOOL, (+/-)- 
ALOE VERA LEAF 
SODIUM HYDROXIDE 
Packaging
#Item CodePackage Description
1NDC:49967-799-01250 mL in 1 BOTTLE
2NDC:49967-799-025 mL in 1 PACKET
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358H06/04/2012
Labeler - L'Oreal USA Products Inc (002136794)
Establishment
NameAddressID/FEIOperations
L'Oreal USA, Inc.185931458manufacture(49967-799)

Revised: 01/2020
 
L'Oreal USA Products Inc

Further information

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