LOreal Paris Ever Pure Dandruff Scalp Care and Detox

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Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Pyrithone zinc 1%

Purpose

OTC - PURPOSE SECTION

Antidandruff

Use

INDICATIONS & USAGE SECTION

helpls prevent recurrence of scalp flaking and itching associated with dandruff

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

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

Stop use and ask a doctor if

OTC - STOP USE SECTION

condition worsens or does not improve after regular use

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

• for best results, use at least twice a week or as directed by a doctor
• apply to wet hair by gently massaging onto scalp and hair
• rinse well

Inactive ingredients

INACTIVE INGREDIENT SECTION

water, cocamidopropyl betaine, disodium laureth sulfosuccinate, sodium lauryl sulfoacetate, decyl glucoside, sodium lauroyl sarcosinate, glycol distearate, sodium chloride, coco-betaine, fragrance, amodimethicone, PPG-5-ceteth-20, acrylates copolymer, sodium benzoate, carbomer, PEG-55 propylene glycol oleate, propylene glycol, polyquaternium-39, menthol, hydrogenated starch hydrolysate, benzoic acid, trideceth-6, butylene glycol, citronellol, sodium polynaphthalenesulfonate, linalool, limonene, geraniol, cetrimonium chloride, citral, cellulose gum, tetrasodum EDTA, aphanizomenon flos-aquae extract, melia azadirachta leaf extract, methylisothiazolinone, phenoxyethanol, potassium sorbate

Questions or comments?

OTC - QUESTIONS SECTION

1-800-631-7358

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 37 matching rows.

• LOreal Paris Ever Pure Dandruff Scalp Care and Detox
• Pyrithione Zinc
• WATER
• COCAMIDOPROPYL BETAINE
• DISODIUM LAURETH SULFOSUCCINATE
• SODIUM LAURYL SULFOACETATE
• DECYL GLUCOSIDE
• SODIUM LAUROYL SARCOSINATE
• GLYCOL DISTEARATE
• SODIUM CHLORIDE
• COCO-BETAINE
• AMODIMETHICONE (1300 CST)
• PPG-5-CETETH-20
• SODIUM HYDROXIDE
• CITRIC ACID MONOHYDRATE
• SODIUM BENZOATE
• CARBOMER 940
• PROPYLENE GLYCOL
• POLYQUATERNIUM-39 (22.5/51/26.5 ACRYLIC ACID/ACRYLAMIDE/DADMAC; 1600000 MW)
• MENTHOL
• HYDROGENATED STARCH HYDROLYSATE
• BENZOIC ACID
• TRIDECETH-6
• BUTYLENE GLYCOL
• .BETA.-CITRONELLOL, (R)-
• LINALOOL, (+/-)-
• LIMONENE, (+)-
• GERANIOL
• CETRIMONIUM CHLORIDE
• CITRAL
• CARBOXYMETHYLCELLULOSE SODIUM (0.7 CARBOXYMETHYL SUBSTITUTION PER SACCHARIDE; 150 MPA.S AT 1%)
• EDETATE SODIUM
• APHANIZOMENON FLOSAQUAE
• AZADIRACHTA INDICA LEAF
• METHYLISOTHIAZOLINONE
• PHENOXYETHANOL
• POTASSIUM SORBATE

NDC Codes#

Ingredients#

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DailyMed ingredient rows page 1 of 1 · 36 matching rows.

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Matched openFDA labels page 1 of 1 · 1 matching rows.

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Adverse event summaries are temporarily unavailable. Other product information remains available.