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CVS Decolorized Iodine

Medically reviewed on December 15, 2017

Dosage form: liquid
Ingredients: ALCOHOL 0.48mL in 1mL
Labeler: CVS Pharmacy
NDC Code: 69842-207

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.

CVS Decolorized Iodine

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)

CVS DECOLORIZED IODINE 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69842-207
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.48 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIA 
IODINE 
POTASSIUM IODIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:69842-207-9259 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2008
Labeler - CVS Pharmacy (062312574)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884analysis(69842-207), manufacture(69842-207), pack(69842-207), label(69842-207)

 
CVS Pharmacy

Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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