OTC Medication Information: L OCCITANE Anti-Dandruff Sensitive Scalp

L OCCITANE ANTI-DANDRUFF SENSITIVE SCALP — pyrithione zinc shampoo
Laboratoires M&L

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.

L’OCCITANE Anti-Dandruff Shampoo Sensitive Scalp

Active Ingredients

ZINC PYRITHIONE 1%

Purpose

Anti-dandruff

Uses

  • Helps eliminate and prevent recurrence of the symptoms of dandruff

Warnings

  • For external use only

When using this product

  • Avoid contact with the eyes. If contact occurs, rinse eyes thoroughly with water.

If condition

worsens or does not improve after regular use of this product as directed, consult a doctor.

Keep out the reach of children.

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

Directions

  • Apply evenly to scalp, leave on for a few minutes, and then rinse off.
  • For best result use at least twice a week or as directed by a doctor.

Inactive ingredients

AQUA/WATER — SODIUM LAURETH SULFATE — COCAMIDOPROPYL BETAINE — ACRYLATES COPOLYMER — MENTHA PIPERITA (PEPPERMINT) OIL — MELALEUCA ALTERNIFOLIA (TEA TREE) LEAF OIL — JUNIPERUS MEXICANA OIL — LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL — CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL — MENTHA VIRIDIS (SPEARMINT) LEAF OIL — THYMUS VULGARIS (THYME) OIL — PANTHENOL — HYDROGENATED PALM GLYCERIDES — CITRATE — GLYCERYL OLEATE — COCO-GLUCOSIDE — PEG-7 GLYCERYL COCOATE — POLYQUATERNIUM-10 — CELLULOSE GUM — ISOPROPYL ALCOHOL — SODIUM POLYNAPHTHALENESULFONATE — POTASSIUM SORBATE — SODIUM BENZOATE — METHYLISOTHIAZOLINONE — CITRIC ACID — SODIUM ACETATE — TOCOPHEROL — PARFUM/FRAGRANCE — LIMONENE — LINALOOL — COUMARIN.

L’OCCITANE Anti-Dandruff Shampoo Sensitive Scalp 300ml (10345-035-01)

Shampoo
(click image for full-size original)

L OCCITANE ANTI-DANDRUFF SENSITIVE SCALP
pyrithione zinc shampoo
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:10345-035
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
PYRITHIONE ZINC (PYRITHIONE ZINC) PYRITHIONE ZINC 10 mg in 1 mL
Inactive Ingredients
Ingredient Name Strength
WATER
SODIUM LAURETH-3 SULFATE
COCAMIDOPROPYL BETAINE
PEPPERMINT OIL
TEA TREE OIL
JUNIPERUS DEPPEANA WOOD OIL
LAVENDER OIL
CITRUS MAXIMA FRUIT RIND OIL
SPEARMINT OIL
THYME OIL
PANTHENOL
HYDROGENATED PALM GLYCERIDES
CITRIC ACID MONOHYDRATE
GLYCERYL OLEATE
COCO GLUCOSIDE
PEG-7 GLYCERYL COCOATE
CARBOXYMETHYLCELLULOSE SODIUM
ISOPROPYL ALCOHOL
POTASSIUM SORBATE
SODIUM BENZOATE
METHYLISOTHIAZOLINONE
SODIUM ACETATE
TOCOPHEROL
LINALOOL, (+/-)-
COUMARIN
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:10345-035-01 1 BOTTLE (BOTTLE) in 1 PACKAGE contains a BOTTLE
1 300 mL in 1 BOTTLE This package is contained within the PACKAGE (10345-035-01)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC monograph final part358H 03/05/2014
Labeler — Laboratoires M&L (262533623)
Establishment
Name Address ID/FEI Operations
Laboratoires M&L 262533623 manufacture (10345-035)

Revised: 03/2014 Laboratoires M&L

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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