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Quality Choice Iodides Tincture

Dosage form: liquid
Ingredients: ALCOHOL 0.45mL in 1mL
Labeler: Chain Drug Market Association
NDC Code: 63868-331

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.

Quality Choice Iodides Tincture

Drug Facts

Active Ingredients

Alcohol 45 % denatured with ammonia, Ammonium and Potassium Iodides.

Purpose

Antiseptic

Uses

First aid 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, 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 the reach of children.

In case of acidental ingestion give milk, then give a starch solution made by mixing two tablespoonfools of cornstarch or flour to a pint of water. contact a poison Control Center immediately.

Directions

Clean the affected area. Aply a small amount to the affected area 1 to 3 times daily. May be covered with a sterile bandage. If bandaged, let it dry first.

Inactive Ingredient:

Purified Water

Other Information:

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

Principal Package Display

Label

QUALITY CHOICE IODIDES TINCTURE 
ethyl alcohol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63868-331
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ALCOHOL (ALCOHOL) ALCOHOL0.45 mL  in 1 mL
Inactive Ingredients
Ingredient NameStrength
AMMONIA 
IODINE 
POTASSIUM IODIDE 
WATER 
Packaging
#Item CodePackage Description
1NDC:63868-331-0260 mL in 1 BOTTLE, PLASTIC
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A03/25/1998
Labeler - Chain Drug Market Association (011920774)
Registrant - Humco Holding Group, Inc. (825672884)
Establishment
NameAddressID/FEIOperations
Humco Holding Group, Inc.825672884manufacture(63868-331), analysis(63868-331), pack(63868-331), label(63868-331)

Revised: 12/2017
 
Chain Drug Market Association

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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