CVS DECOLORIZED IODINE- alcohol liquid

CVS Decolorized Iodine by

Drug Labeling and Warnings

CVS Decolorized Iodine by is a Otc medication manufactured, distributed, or labeled by CVS Pharmacy, Pharma Nobis, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

CVS Decolorized Iodine

Drug Facts

Active Ingredient

Alcohol 48%

Purpose

Antiseptic

Uses

To help prevent infection in in minor: cuts, scrapes and burns.

Warnings

Ask a doctor before use if you have

deep or puncture wounds. Animal bites. Serious burns. 

Stop use and consult a doctor if

Condition persists or gets worse, or if using this product for more than 1 week.

For external use only. Do not use in the 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, give milk, then a starch solution made by mixing two tablespoonfuls of cornstarch or flour to a pint of water, Contact a 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

Ammonia, iodine, potassium iodide, purified water.

Other information

Will stain skin and clothing

Flammable

Keep away from spark, heat and flame

PRINCIPAL DISPLAY PANEL

Decolorized
Iodine
First Aid Antiseptic
2 FL OZ (59 mL)

INGREDIENTS AND APPEARANCE

CVS DECOLORIZED IODINE 
alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-207
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
AMMONIA (UNII: 5138Q19F1X)
IODINE (UNII: 9679TC07X4)
POTASSIUM IODIDE (UNII: 1C4QK22F9J)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 69842-207-92	59 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	01/01/2008

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part333A	01/01/2008

Labeler - CVS Pharmacy (062312574)

Registrant - Humco Holding Group, Inc. (825672884)

Establishment
Name	Address	ID/FEI	Business Operations
Humco Holding Group, Inc.		825672884	analysis(69842-207) , manufacture(69842-207) , pack(69842-207) , label(69842-207)