MILD IODINE TINCTURE- iodine and sodium iodide and alcohol liquid

mild iodine tincture by

Drug Labeling and Warnings

mild iodine tincture by is a Otc medication manufactured, distributed, or labeled by 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. Will stain skin and clothing.

DO NOT USE

Do not use longer than 1 week unless directed by a doctor.

ASK DOCTOR

Ask a doctor before use if 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.

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?

1-888-235-2466

SPL UNCLASSIFIED SECTION

Manufactured for: Bionpharma Inc., Princeton, NJ 08540

R0525 L0001035

1 fl oz. bottle label

a+ health TM

mild

iodine

tincture, 2%

alcohol 47%

first aid antiseptic

• helps prevent infection in minor cuts, scrapes & burns

flammable: Keep away

from fire or flame.

1 fl oz (30 mL)

INGREDIENTS AND APPEARANCE

MILD IODINE TINCTURE 
iodine and sodium iodide and alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69452-484
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: 69452-484-36	30 mL in 1 BOTTLE; Type 0: Not a Combination Product	10/06/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	10/06/2025

Labeler - BIONPHARMA INC. (079637826)

Registrant - BIONPHARMA INC. (079637826)

Establishment
Name	Address	ID/FEI	Business Operations
Pharma Nobis, LLC		118564114	manufacture(69452-484)