EQUATE description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

EQUATE

Wal-Mart Stores Inc.
APOLLO HEALTH AND BEAUTY CARE

DRUG FACTS


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

ACTIVE INGREDIENT

SELENIUM SULFIDE 1%

PURPOSE

ANTI-DANDRUFF, ANTI-SEBORRHEIC DERMATITIS

USES

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

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 PRODUCT GETS INTO EYES, RINSE THOROUGHLY WITH WATER. FOR USE ON COLOR TREATED OR PERMED HAIR, RINSE THOROUGHLY.

STOP USING THIS PRODUCT 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 A POISON CONTROL CENTER IMMEDIATELY.

DIRECTIONS

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

INACTIVE INGREDIENTS

WATER (AQUA), AMMONIUM LAURETH SULFATE, AMMONIUM LAURYL SULFATE, GLYCOL DISTEARATE, COCAMIDE MEA, ACRYLATES COPOLYMER, AMMONIUM XYLENESULFONATE, 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).

QUESTIONS?

1-888-287-1915

LABEL COPY

EQUATE

EQUATE

SELENIUM SULFIDE LIQUID

Product Information

Product Type Human otc drug label Item Code (Source) NDC:49035-618
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
SELENIUM SULFIDE SELENIUM SULFIDE 10 mg

Inactive Ingredients

Ingredient Name Strength
water
AMMONIUM LAURETH-3 SULFATE
Ammonium Lauryl Sulfate
GLYCOL DISTEARATE
COCO MONOETHANOLAMIDE
METHACRYLIC ACID - METHYL METHACRYLATE COPOLYMER (1:1)
AMMONIUM XYLENESULFONATE
SODIUM CITRATE
DIMETHICONE
CETYL ALCOHOL
SODIUM CHLORIDE
CITRIC ACID MONOHYDRATE
SODIUM BENZOATE
stearyl alcohol
EDETATE DISODIUM
HYPROMELLOSES
METHYLCHLOROISOTHIAZOLINONE
METHYLISOTHIAZOLINONE
FD&C RED NO. 4

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:49035-618-14 420 in 1 BOTTLE, PLASTIC

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partH part358H 2012-09-19


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.