Lugols Strong Iodine

LUGOLS STRONG IODINE- iodine and potassium iodide solution
CooperSurgical, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

CONTENTS

Iodine 0.05 g/ml, Potassium Iodide 0.100 g/ml.

DESCRIPTION

LUGOL’S is an aqueous solution containing Iodine 5%, and potassium iodide 10%, w/v (LUGOL’s Solution). LUGOL’s is a transparent liquid with a deep brown color and the odor of iodine.

HOW SUPPLIED

LUGOL’S is supplied in 8 ml glass single-use bottles.

INDICATIONS AND USAGE

LUGOL’s is a topical antiseptic. Strong Iodine Solution is a germicide and fungicide. LUGOL’s is preservative-free.

ADMINISTRATION

LUGOL’S is applied directly to areas needing antiseptic.

WARNINGS

For External Use Only.

CONTRAINDICATIONS

Iodide preparations are contraindicated in patients with known sensitivity to the drugs.

CAUTION

Federal law restricts this device to sale by or on the order of a physician.

STORAGE

Keep tightly closed. Protect from light. DO NOT use if seal has been broken. Store at controlled room temperature 15°-30°C (59°-86°F).

DISPOSAL

Opened containers with unused portions of product and applicator swabs containing residual product should be placed in a suitable, dry container for disposal following local hazardous waste practices. Waste containing LUGOL’S should not be subjected to any thermal process whether intended for destruction or recycling purposes.

PRINCIPAL DISPLAY PANEL

Lugol’s
Strong Iodine Solution USP

Contents

One Dozen (12)

8ml Vials

Lugol’s Strong Iodine Solution USP Contents One Dozen (12) 8ml Vials
(click image for full-size original)

PRINCIPAL DISPLAY PANEL

8mL NDC 59365-6064-0
Lugol’s

(STRONG IODINE SOLUTIONS USP)

PRINCIPAL DISPLAY PANEL
8mL       NDC 59365-6064-0
Lugol’s 
(STRONG IODINE SOLUTIONS USP)
(click image for full-size original)
LUGOLS STRONG IODINE
iodine and potassium iodide solution
Product Information
Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:59365-6064
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
IODINE (IODINE) IODINE 0.05 g in 1 mL
POTASSIUM IODIDE (IODIDE ION) POTASSIUM IODIDE 0.100 g in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:59365-6064-1 12 VIAL, SINGLE-USE in 1 CARTON contains a VIAL, SINGLE-USE (59365-6064-0)
1 NDC:59365-6064-0 8 mL in 1 VIAL, SINGLE-USE This package is contained within the CARTON (59365-6064-1)
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED DRUG OTHER 10/01/1992
Labeler — CooperSurgical, Inc. (801895244)

Revised: 05/2016 CooperSurgical, Inc.

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