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Health Mart Iodides

Medically reviewed on December 3, 2017

Dosage form: liquid
Ingredients: ALCOHOL 0.48mL in 1mL
Labeler: McKesson
NDC Code: 62011-0116

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.

Health Mart Decolorized Iodine

Health Mart Iodides Tincture

Drug Facts

Active Ingredient

Alcohol 48% v/v

Purpose

Antiseptic

Uses

To help prevent infection in 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 consult a doctor if:

Condition persists or gets worse, or if using this product for more 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 a starch solution made by mixing two tablespoons 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

Health Mart Pharmacy
iodine tincture
(decolorized iodine)
2 FL OZ (59 mL)

Label

HEALTH MART IODIDES 
alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62011-0116
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:62011-0116-159 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A01/01/2008
Labeler - McKesson (177667227)
Registrant - Humco Holding Gruop, Inc (825672884)
Establishment
NameAddressID/FEIOperations
Humco Hlding Group, Inc.825672884manufacture(62011-0116), analysis(62011-0116), pack(62011-0116), label(62011-0116)

 
McKesson

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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