IODO BLANCO (IODINE TINCTURE DECOLORIZED) FIRST AID ANTISEPTIC- iodine 2% liquid

Iodo Blanco (Iodine Tincture Decolorized) by

Drug Labeling and Warnings

Iodo Blanco (Iodine Tincture Decolorized) by is a Otc medication manufactured, distributed, or labeled by Germa Products, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Iodine Tincture Decolorized 2%

Purpose

First aid antiseptic

Uses

As a first aid to help prevent skin infection in n minor cuts n scrapes n burns
Warnings For external use only

Warnings

For external use only
Ask a doctor before use. if you have deep or puncture wounds, animal bites or serious burns. When using this product. do not use in eyes or apply over large areas of the body. do not use longer than 1 week unless directed by a doctor.
Stop use and ask a doctor if condition persists or gets worse

Ask a Doctor before use if

If you have deep or puncture wounds, animal bites or serious burns.

Keep out of reach of children.

Keep out of the reach of children. If swallowed, get medical
help or contact a Poison Control Center right away.

Directions

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

Other Information

Product will stain skin and clothing.

Inactive Ingredients

Ethyl alcohol, ammonia, sodium iodine, water.

Questions or Comments

1-305-256-1464

Principal Display Panel

Iodo Blanco

INGREDIENTS AND APPEARANCE

IODO BLANCO (IODINE TINCTURE DECOLORIZED)  FIRST AID ANTISEPTIC
iodine 2% liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73635-1222
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

Inactive Ingredients
Ingredient Name	Strength
AMMONIA (UNII: 5138Q19F1X)
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)
SODIUM IODIDE (UNII: F5WR8N145C)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73635-1222-1	30 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	03/29/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M003	03/29/2021

Labeler - Germa Products, LLC (116626935)

Registrant - Germa Products, LLC (116626935)