Drug Facts

Drug Facts
SPL v1
SPL
SPL Set ID 9f8f976b-9e5e-4f18-baac-a1f0adaa7738
Route
TOPICAL
Published
Effective Date 2013-03-20
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Identifiers & Packaging


Description

Active Ingredient Pyrithione Zinc 1%


Medication Information

Warnings and Precautions

W arnings For external use only

Indications and Usage

Uses • helps eliminate irritation and flaking associated with dandruff.

Dosage and Administration

Directions •wet hair •lather •massage onto scalp •rinse well •repeat if desired •for best results use regularly

Description

Active Ingredient Pyrithione Zinc 1%

Section 50565-1

Keep this and all drugs out of reach of children If swallowed get medical help or contact a Poison Control Center right away.

Section 50566-9

Stop use and ask a doctor if condition does not improve or worsen after regular use of this product as directed

Section 50567-7

When using this product •avoid contact with eyes • if contact occurs, rinse eyes with plenty of water.

Section 51727-6

Inactive Ingredients acrylates copolymer, benzyl alcohol, cetyl alcohol, citric acid, cocamide MEA, dimethicone, fragrance, glycol distearate, guar hydroxypropyltrimonium chloride, methylchloroisothiazolinone, methylisothiazolinone, prunus amygdalus dulcis (sweet almond) oil, sodium chloride, sodium laureth sulfate, sodium lauryl sulfate, triethanolamine, water, zinc sulfate 

Section 51945-4

image description

Section 55105-1

Purpose Anti-Dandruff

Section 55106-9

Active Ingredient Pyrithione Zinc 1%


Structured Label Content

Indications and Usage (34067-9)

Uses • helps eliminate irritation and flaking associated with dandruff.

Dosage and Administration (34068-7)

Directions •wet hair •lather •massage onto scalp •rinse well •repeat if desired •for best results use regularly

Warnings and Precautions (34071-1)

W arnings For external use only

Section 50565-1 (50565-1)

Keep this and all drugs out of reach of children If swallowed get medical help or contact a Poison Control Center right away.

Section 50566-9 (50566-9)

Stop use and ask a doctor if condition does not improve or worsen after regular use of this product as directed

Section 50567-7 (50567-7)

When using this product •avoid contact with eyes • if contact occurs, rinse eyes with plenty of water.

Section 51727-6 (51727-6)

Inactive Ingredients acrylates copolymer, benzyl alcohol, cetyl alcohol, citric acid, cocamide MEA, dimethicone, fragrance, glycol distearate, guar hydroxypropyltrimonium chloride, methylchloroisothiazolinone, methylisothiazolinone, prunus amygdalus dulcis (sweet almond) oil, sodium chloride, sodium laureth sulfate, sodium lauryl sulfate, triethanolamine, water, zinc sulfate 

Section 51945-4 (51945-4)

image description

Section 55105-1 (55105-1)

Purpose Anti-Dandruff

Section 55106-9 (55106-9)

Active Ingredient Pyrithione Zinc 1%


Raw Label Data

All Sections (JSON)