EPSAL- magnesium sulfate, unspecified form ointment

Epsal by

Drug Labeling and Warnings

Epsal by is a Otc medication manufactured, distributed, or labeled by Press Chemical and Pharmaceutical Laboratories. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INDICATIONS & USAGE

Epsal Ointment, a Specially Suspended Epsom Salts Drawing Ointment is Recommended for External Application to draw foreign substances from below the surface of the skin, as for example, a sliver of wood or a stinger from a bee bite.

DIRECTIONS

Apply a heaping quantity to affected parts one or two times a day. Bandage loosely to protect the clothing if necessary.

Active Ingredient

Magnesium Sulfate 40%.

Inactive Ingredients

Purified Water, White Petrolatum, Mineral Oil, Microcrystalline Wax, Lanolin Alcohol

WARNINGS

FOR EXTERNAL USE ONLY. CAUTION: In case of deep or puncture wounds or serious burns, consult physician. If redness, irritation, swelling or pain persists or increases or if infection occurs, discontinue use and consult physician.

WARNING

KEEP OUT OF REACH OF CHILDREN

SPL UNCLASSIFIED SECTION

NDC #11649-0001-3

Distributed By
PRESS CHEMICAL & PHARMACEUTICAL LAB
COLUMBUS, OHIO 43209

PRINCIPAL DISPLAY PANEL - 60 gram Jar Label

Epsal®
OINTMENT

NET WT. 2 OZ. (60 grams)

INGREDIENTS AND APPEARANCE

EPSAL 
magnesium sulfate, unspecified form ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11649-0001
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
Magnesium Sulfate, Unspecified Form (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838)	Magnesium Sulfate, Unspecified Form	400 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
Petrolatum (UNII: 4T6H12BN9U)	143 mg  in 1 g
Mineral Oil (UNII: T5L8T28FGP)
Microcrystalline Wax (UNII: XOF597Q3KY)
Lanolin Alcohols (UNII: 884C3FA9HE)

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11649-0001-3	12 in 1 BOX	01/15/1957
1		60 g in 1 JAR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part334	01/15/1957

Labeler - Press Chemical and Pharmaceutical Laboratories (059935494)