IODO ALBO IODIDE- alcohol liquid liquid

Iodo Albo Iodide by

Drug Labeling and Warnings

Iodo Albo Iodide by is a Otc medication manufactured, distributed, or labeled by Menper Distributors Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

DOSAGE & ADMINISTRATION

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.

ACTIVE INGREDIENT

Ethyl Alcohol 48%

INDICATIONS & USAGE

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

WARNINGS

For External Use Only.

When using this product:

Do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites or serious burns consult a doctor.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) immediately. Soap will deactivate the effects of this product.

INACTIVE INGREDIENT

• Ammonium Hydroxide
• Iodine
• Potassium Iodide
• Purified Water

PURPOSE

First Aid Antiseptic

Iodo Albo Iodide

INGREDIENTS AND APPEARANCE

IODO ALBO IODIDE 
alcohol liquid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53145-120
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	0.48 mL  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
IODINE (UNII: 9679TC07X4)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
AMMONIA (UNII: 5138Q19F1X)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 53145-120-91	30 mL in 1 CONTAINER; Type 0: Not a Combination Product	04/09/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	04/09/2019

Labeler - Menper Distributors Inc. (101947166)