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Sunmark Iodine

Dosage form: tincture
Ingredients: IODINE 20mg in 1mL, SODIUM IODIDE 20.4mg in 1mL, ALCOHOL 470mg in 1mL
Labeler: McKesson
NDC Code: 49348-133

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.

sunmark Iodine Tincture USP 2%

sunmark Iodine Tincture USP 2%

Active Ingredients

Iodine  2%,  Sodium Iodide 2.4%,  Alcohol 47%




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


For external use only.

Ask a doctor before use if you have
  • deep or puncture wounds
  • animal bites
  • serious burns.

Stop use ask a doctor if
  • condition persists or gets worse, or 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 tablespoonfuls of cornstarch or flour to a pint of water.  Contact a Poison Control Center immediately.


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:

Purified Water.

Other information:

Will stain skin and clothing.   FLAMMABLE:  Keep away from spark, heat and flame.

sunmark  iodine tincture USP 2%  First aid antiseptic Alcohol 47%  Distributed by McKesson One Post Street, San Francisco, CA 94104  Money Back Guarantee  1 FL OZ (30 mL)

sunmark Iodine Tincture USP 2% 1oz (49348-133-27)

iodine, sodium iodide, alcohol tincture
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49348-133
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Inactive Ingredients
Ingredient NameStrength
#Item CodePackage Description
1NDC:49348-133-2730 mL in 1 BOTTLE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart333A06/28/2012
Labeler - McKesson (177667227)
Humco Holding Group, Inc.825672884manufacture

Revised: 07/2012

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.