EPSAL- magnesium sulfate, unspecified form ointment 
Press Chemical and Pharmaceutical Laboratories

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Epsal Ointment

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

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

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)

Principal Display Panel - 60 gram Jar Label
EPSAL 
magnesium sulfate, unspecified form ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11649-0001
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Magnesium Sulfate, Unspecified Form (UNII: DE08037SAB) (MAGNESIUM CATION - UNII:T6V3LHY838) Magnesium Sulfate, Unspecified Form400 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Petrolatum (UNII: 4T6H12BN9U) 143 mg  in 1 g
Mineral Oil (UNII: T5L8T28FGP)  
Microcrystalline Wax (UNII: XOF597Q3KY)  
Lanolin Alcohols (UNII: 884C3FA9HE)  
Product Characteristics
ColorWHITEScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11649-0001-312 in 1 BOX01/15/1957
160 g in 1 JAR; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart33401/15/1957
Labeler - Press Chemical and Pharmaceutical Laboratories (059935494)

Revised: 1/2020
Document Id: 45ca291b-91e5-47c0-baf0-1fce22c12ced
Set id: 6601b210-3d9f-49da-a6a1-27691596b29c
Version: 2
Effective Time: 20200124
 
Press Chemical and Pharmaceutical Laboratories