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HUMCO 1 Percent Iodine

Medically reviewed on Nov 13, 2017

Dosage form: liquid
Ingredients: ISOPROPYL ALCOHOL 700mg in 1mL
Labeler: Humco Holding Group, Inc.
NDC Code: 0395-1211

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.

Iodine Tincture 1 percent

HUMCO 1% Iodine Tincture

Drug Facts

Active Ingredient

Isopropyl Alcohol 70%

Purpose

Topical antiseptic

Indications

Preoperative skin preparation. Helps to reduce skin bacteria that potentially can cause skin infection.

Warnings:

Flammable: Keep away from spark, heat or flame.

Do not use with electrocautery procedures.

For external use only.

Do not use

in the eyes  

Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

IF ON SKIN: Wash with plenty of soap and water.

IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. If skin irritation or rash occurs of if eye irritation persists, get medical advice/attention. Take off contaminated clothing and wash before reuse.

IN CASE OF FIRE: Use dry sand, dry chemical or alcohol resistant foam to extinguish. Store in well ventilated place. Keep cool. Dispose contents/container to an approved waste disposal plant.

Keep out of reach of children.

If swallowed get medical help or contact a Poison Control Center right away.

Directions
  • Use only by trained personnel.
  • Clean the affected area.
  • Apply product to operative site prior to surgery.
  • When this product dries remove immediately with 70% alcohol or as directed by a physician.

Other Information

Will stain skin and clothing. Store at room temperature.

Inactive Ingredient

Iodine 1%, Potassium iodide, Purified water.

PRINCIPAL DISPLAY PANEL

NDC 0395-1211-16
1 % IODINE
TINCTURE
16 FL OZ
(1 PT) 473 mL

HUMCO 1 PERCENT IODINE 
isopropyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0395-1211
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ISOPROPYL ALCOHOL (ISOPROPYL ALCOHOL) ISOPROPYL ALCOHOL700 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
IODINE10 mg  in 1 mL
POTASSIUM IODIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:0395-1211-16473 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A06/08/2017
Labeler - Humco Holding Group, Inc. (825672884)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884manufacture(0395-1211), pack(0395-1211), analysis(0395-1211), label(0395-1211)

 
Humco Holding Group, Inc.

Further information

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

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