TOPCARE GENTLE DANDRUFF CLINICAL STRENGTH SELENIUM SULFIDE SELENIUM SULFIDE SELENIUM SULFIDE WATER AMMONIUM LAURETH-3 SULFATE AMMONIUM LAURYL SULFATE GLYCOL DISTEARATE COCO MONOETHANOLAMIDE AMMONIUM XYLENESULFONATE METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) SODIUM HYDROXIDE SODIUM CITRATE DIMETHICONE CETYL ALCOHOL SODIUM CHLORIDE CITRIC ACID MONOHYDRATE SODIUM BENZOATE STEARYL ALCOHOL EDETATE DISODIUM HYPROMELLOSES METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE FD&C RED NO. 4 USES HELPS PREVENT THE CHANCE OF RECURRENCE OF FLAKING, ITCHING, IRRITATION, SCALING AND REDNESS ASSOCIATED WITH DANDRUFF AND SEBORRHEIC DERMATITIS

TOPCARE GENTLE DANDRUFF CLINICAL STRENGTH SELENIUM SULFIDE SELENIUM SULFIDE SELENIUM SULFIDE WATER AMMONIUM LAURETH-3 SULFATE AMMONIUM LAURYL SULFATE GLYCOL DISTEARATE COCO MONOETHANOLAMIDE AMMONIUM XYLENESULFONATE METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1) SODIUM HYDROXIDE SODIUM CITRATE DIMETHICONE CETYL ALCOHOL SODIUM CHLORIDE CITRIC ACID MONOHYDRATE SODIUM BENZOATE STEARYL ALCOHOL EDETATE DISODIUM HYPROMELLOSES METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE FD&C RED NO. 4

Mfr: OTC
FunFoxMeds box

Drug Facts

Composition & Profile

Active Ingredients
ACTIVE INGREDIENT SELENIUM SULFIDE 1% PURPOSE ANTI-DANDRUFF ANTI-SEBORRHEIC DERMATITIS
Inactive Ingredients
INACTIVE INGREDIENTS WATER (AQUA) AMMONIUM LAURETH SULFATE AMMONIUM LAURYL SULFATE GLYCOL DISTEARATE COCAMIDE MEA AMMONIUM XYLENESULFONATE ACRYLATES COPOLYMER SODIUM HYDROXIDE SODIUM CITRATE FRAGRANCE (PARFUM) DIMETHICONE CETYL ALCOHOL SODIUM CHLORIDE CITRIC ACID SODIUM BENZOATE STEARYL ALCOHOL DISODIUM EDTA HYDROXYPROPYL METHYLCELLULOSE METHYLCHLOROISOTHIAZOLINONE METHYLISOTHIAZOLINONE RED 4 (CI 14700)
Strengths
1 %
Treats Conditions
Uses Helps Prevent The Chance Of Recurrence Of Flaking Itching Irritation Scaling And Redness Associated With Dandruff And Seborrheic Dermatitis

Identifiers & Packaging

Container Type UNKNOWN
Packaging

LABEL COPY IMAGE OF THE LABEL

Package Descriptions
  • LABEL COPY IMAGE OF THE LABEL

Overview

USES HELPS PREVENT THE CHANCE OF RECURRENCE OF FLAKING, ITCHING, IRRITATION, SCALING AND REDNESS ASSOCIATED WITH DANDRUFF AND SEBORRHEIC DERMATITIS

Indications & Usage

USES HELPS PREVENT THE CHANCE OF RECURRENCE OF FLAKING, ITCHING, IRRITATION, SCALING AND REDNESS ASSOCIATED WITH DANDRUFF AND SEBORRHEIC DERMATITIS

Dosage & Administration

DIRECTIONS SHAKE WELL. APPLY SHAMPOO, RINSE THOROUGHLY. FOR BEST RESULTS, USE AT LEAST TWICE A WEEK OR AS DIRECTED BY A DOCTOR

Warnings & Precautions
WARNINGS FOR EXTERNAL USE ONLY ASK A DOCTOR BEFORE USING IF YOU HAVE SEBORRHEIC DERMATITIS IN AREAS OTHER THAN THE SCALP WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. FOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY STOP USE AND ASK A DOCTOR IF CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY
Purpose

PURPOSE ANTI-DANDRUFF, ANTI-SEBORRHEIC DERMATITIS

When Using

WHEN USING THIS PRODUCT AVOID CONTACT WITH EYES. IF CONTACT OCCURS, RINSE EYES THOROUGHLY WITH WATER. FOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY STOP USE AND ASK A DOCTOR IF CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

Stop Use & Ask a Doctor

STOP USE AND ASK A DOCTOR IF CONDITION WORSENS OR DOES NOT IMPROVE AFTER REGULAR USE OF THIS PRODUCT AS DIRECTED IN CASE OF ACCIDENTAL INGESTION, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER IMMEDIATELY

Keep Out of Reach of Children

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


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