CVS IODINE- iodine, sodium iodide and alcohol liquid

CVS Iodine by

Drug Labeling and Warnings

CVS 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 Iodine Tincture USP

Drug Facts

Active Ingredient

Iodine 2%

Sodium Iodide 2.4%

Alcohol 47%

Purpose

Antiseptic

Indications

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

Warnings:

For external use only

Ask a doctor before use if you have

Deep or puncture wounds

Animal bites

Serious burns

Stop use and ask a doctor if

the condition persists or gets worse, if using this product for longer than 1 week.

When using this product

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 give a starch solution made by mixing two tablespoofuls of cornstarch or flour to a pint of water. Contact a Poison Control Center immediately.

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.

Inactive Ingredient

Purified water.

Other Information

Will stain skin and clothing

     

PRINCIPAL DISPLAY PANEL

CVS Health

Iodine Tincture USP

First Aid Antiseptic

1 FL OZ (30 mL)

INGREDIENTS AND APPEARANCE

CVS IODINE 
iodine, sodium iodide and alcohol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 69842-213
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
SODIUM IODIDE (UNII: F5WR8N145C) (IODIDE ION - UNII:09G4I6V86Q)	IODIDE ION	20.4 mg  in 1 mL
ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M)	ALCOHOL	470 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: 69842-213-91	30 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	manufacture(69842-213) , analysis(69842-213) , pack(69842-213) , label(69842-213)