MILD IODINE TINCTURE- iodine and sodium iodine and alcohol liquid

mild iodine tincture by

Drug Labeling and Warnings

mild iodine tincture by is a Otc medication manufactured, distributed, or labeled by KROGER COMPANY, BIONPHARMA INC., Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

IodineTincture USP 2%

Purpose

First Aid Antiseptic

Uses

First aid to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only.

Flammable, Keep away from fire or flame,

DO NOT USE

Do not uselonger than 1 week unless directed by a doctor.

ASK DOCTOR

Ask a doctor before useif you have, deep or punture wounds, animal bites, or serious burns.

Stop use and ask a doctor if

the condition persists or gets worse.

When using this product

■ do not use in eyes. If contact occurs flush with large amounts of water while lifting upper and lower lids. ■ do not apply over large areas of the body.

Will stain skin and clothing.

Keep out of reach of children.

In case of accidental ingestion, contact Poison Control Center immediately.

Directions

Clean the affected area. Apply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged let dry first.

Inactive Ingredient

Purified Water

Questions?

1-888-632-6900

SPL UNCLASSIFIED SECTION

PROUDLY DISTRIBUTED BY THE KROGER CO., CINCINNATI, OHIO 45202

R1025 L0001174

1 fl oz. bottle label

Kroger

Iodine 2%

Tincture, USP

Alcohol 47%

first aid antiseptic

For External Use Only

FLAMMABLE POISON

1 fl oz (30 mL)

INGREDIENTS AND APPEARANCE

MILD IODINE TINCTURE 
iodine and sodium iodine and alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59450-030
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
IODINE (UNII: 9679TC07X4) (IODINE - UNII:9679TC07X4)	IODINE	20 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	470 mg  in 1 mL
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20.4 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59450-030-36	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	03/11/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/11/2026

Labeler - KROGER COMPANY (006999528)

Registrant - BIONPHARMA INC. (079637826)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	manufacture(59450-030)