LIQUIMAT ACNE TREATMENT AND COVER-UP- sulfur liquid

LIQUIMAT by

Drug Labeling and Warnings

LIQUIMAT by is a Otc medication manufactured, distributed, or labeled by Summers Laboratories Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

ACTIVE INGREDIENT

SULFUR 4%

PURPOSE

PURPOSE

ACNE TREATMENT LOTION

INDICATIONS & USAGE

USE

DRIES UP ACNE PIMPLES, HELPS PREVENT NEW PIMPLES

WARNINGS

WARNINGS

• FOR EXTERNAL USE ONLY

DO NOT USE

DO NOT USE

• ON BROKEN SKIN
• ON LARGE AREAS OF THE BODY

WHEN USING

WHEN USING THIS PRODUCT

• APPLY TO AFFECTED AREAS ONLY
• DO NOT GET INTO EYES
• USING OTHER TOPICAL ACNE DRUGS AT THE SAME TIME OR RIGHT AFTER USE OF THIS PRODUCT MAY INCREASE DRYNESS OR IRRITATION OF THE SKIN. IF THIS OCCURS, ONLY ONE DRUG SHOULD BE USED UNLESS DIRECTED BY A DOCTOR

STOP USE

STOP USE AND ASK A DOCTOR IF

• TOO MUCH IRRITATION DEVELOPS OR INCREASES

KEEP OUT OF REACH OF CHILDREN. IF SWALLOWED, GET MEDICAL HELP OR CONTACT A POISON CONTROL CENTER RIGHT AWAY.

DOSAGE & ADMINISTRATION

DIRECTIONS

• CLEAN SKIN THOROUGHLY BEFORE USING
• COVER THE ENTIRE AFFECTED AREA WITH A THIN LAYER 1 TO 3 TIMES DAILY
• BECAUSE TOO MUCH DRYING OF THE SKIN MAY OCCUR, START WITH 1 APPLICATION DAILY, THEN INCREASE TO 2 TO 3 TIMES DAILY IF NEEDED OR AS DIRECTED BY A DOCTOR.

INACTIVE INGREDIENT

INACTIVE INGREDIENTS

WATER, SD-40 ALCOHOL 22-PERCENT, KAOLIN, ZINC OXIDE, GLYCERIN, TITANIUM DIOXIDE, TALC, CELLULOSE GUM, MAGNESIUM ALUMINUM SILICATE, CETYL ALCOHOL, POLOXAMER 182, FRAGRANCE, IRON OXIDES. COLOR MATCHER CONTAINS IRON OXIDES, PEG-8, PEG-8 LAURATE, SIMETHICONE.

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

LIQUIMAT  ACNE TREATMENT AND COVER-UP
sulfur liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11086-028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70)	SULFUR	3 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)	22 mL  in 100 mL
KAOLIN (UNII: 24H4NWX5CO)
ZINC OXIDE (UNII: SOI2LOH54Z)
GLYCERIN (UNII: PDC6A3C0OX)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
TALC (UNII: 7SEV7J4R1U)
CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
CETYL ALCOHOL (UNII: 936JST6JCN)
POLOXAMER 182 (UNII: JX0HIX6OAG)
FERRIC OXIDE RED (UNII: 1K09F3G675)
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
PEG-8 LAURATE (UNII: 762O8IWA10)
DIMETHICONE (UNII: 92RU3N3Y1O)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11086-028-01	44 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/30/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part333D	10/30/2013

Labeler - Summers Laboratories Inc (002382612)

Establishment
Name	Address	ID/FEI	Business Operations
Summers Laboratories Inc		002382612	manufacture(11086-028) , pack(11086-028)