Epsal
FDA Label NDC 11649-0001

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Press Chemical And Pharmaceutical Laboratories for the product Epsal (NDC 11649-0001). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.

This specific version of the label includes detailed information regarding otc - purpose, directions, active ingredient, inactive ingredients, warnings, otc - keep out of reach of children, other, principal display panel - 60 gram jar label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

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.

Otc - Keep Out Of Reach Of Children

KEEP OUT OF REACH OF CHILDREN

Other

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)

Principal Display Panel (60 gram Jar Label)

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