IODO ALBO IODIDE- alcohol liquid liquid
Menper Distributors Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Iodo Albo Iodide

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.

Ethyl Alcohol 48%

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

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

Ammonium Hydroxide
Iodine
Potassium Iodide
Purified Water

First Aid Antiseptic

Iodo Albo Iodide

Iodo Albo Iodides.jpg

IODO ALBO IODIDE
alcohol liquid liquid

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

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

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

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

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

Labeler - Menper Distributors Inc. (101947166)