back label - drug facts box

back label - drug facts box
SPL v1
SPL
SPL Set ID aca69d6f-dafc-40d9-a5ce-3fb1279143ab
Route
topical
Published
Effective Date 2010-07-01
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
pyrithione zinc (1 mL)

Identifiers & Packaging

Marketing Status
otc monograph final active Since 2010-07-01
Purpose

ANTI-DANDRUFF

Description

PYRITHIONE ZINC 1%

Medication Information

Warnings

FOR EXTERNAL USE ONLY

Uses
HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF
Purpose
ANTI-DANDRUFF
Directions
FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRE.
Inactive Ingredients

Water (Aqua), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Zinc Carbonate, Glycol Distearate, Fragrance (Parfum), Dimethicone, Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Menthol, PEG-7M, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Sea Salt, Fucus Vesiculosus Extract, Benzyl Alcohol, Sodium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Xylene Sulfonate, Blue 1 (CI 42090), Yellow 5 (CI 19140)

Description

PYRITHIONE ZINC 1%

Active Ingredient

PYRITHIONE ZINC 1%

When Using This Product

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THROUGHLY WITH WATER.

Stop Use and Ask A Doctor If

CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED

Keep Out of Reach of Children

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER IMMEDIATELY.



Package Front and Back Labels

14OZ Front and Back Labels: eq14.jpg

Structured Label Content

Warnings (WARNINGS)

FOR EXTERNAL USE ONLY

Uses
HELPS PREVENT RECURRENCE OF FLAKING AND ITCHING ASSOCIATED WITH DANDRUFF
Purpose (PURPOSE)
ANTI-DANDRUFF
Directions
FOR MAXIMUM DANDRUFF CONTROL, USE EVERY TIME YOU SHAMPOO. WET HAIR, MASSAGE ONTO SCALP AND RINSE. REPEAT IF DESIRE.
Inactive Ingredients

Water (Aqua), Sodium Laureth Sulfate, Sodium Lauryl Sulfate, Cocamide MEA, Zinc Carbonate, Glycol Distearate, Fragrance (Parfum), Dimethicone, Cetyl Alcohol, Polyquaternium-10, Magnesium Sulfate, Sodium Benzoate, Menthol, PEG-7M, Magnesium Carbonate Hydroxide, Ammonium Laureth Sulfate, Sea Salt, Fucus Vesiculosus Extract, Benzyl Alcohol, Sodium Chloride, Methylchloroisothiazolinone, Methylisothiazolinone, Sodium Xylene Sulfonate, Blue 1 (CI 42090), Yellow 5 (CI 19140)

Active Ingredient (ACTIVE INGREDIENT)

PYRITHIONE ZINC 1%

When Using This Product (WHEN USING THIS PRODUCT)

AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THROUGHLY WITH WATER.

Stop Use and Ask A Doctor If (STOP USE AND ASK A DOCTOR IF)

CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED

Keep Out of Reach of Children (KEEP OUT OF REACH OF CHILDREN)

IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT POISON CONTROL CENTER IMMEDIATELY.



Package Front and Back Labels (PACKAGE FRONT AND BACK LABELS)

14OZ Front and Back Labels: eq14.jpg

Advanced Ingredient Data

Raw Label Data

All Sections (JSON)

Additional Information

Back to search View SPL set listing Open on DailyMed ↗

Source: dailymed · Ingested: 2026-02-15T11:55:07.855297 · Updated: 2026-03-14T22:52:28.188101