Active Ingredient
Alcohol 85%
Strong Iodine Tincture
FDA Label NDC 0395-1220
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Humo Holding Group, Inc. for the product Strong Iodine Tincture (NDC 0395-1220). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, ask a doctor if you have:, stop use and consult a doctor if:, when using this product:, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses
To prevent infection in mior cuts, scrapes, and burns.
Warnings
For external use only
Ask A Doctor If You Have:
deep or puncture wounds
animal bites
serious burns.
Stop Use And Consult A Doctor If:
The condition persists or gets worse, or if using for longer than once a week.
When Using This Product:
Do not use in the eyes. If contact occurs, flush with large amounts of water 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 affacted area
Apply a small amount on the area 1 to 3 times daily.
May be covered with sterile bandage.
If bandaged, let it dry first.
Inactive Ingredient
Iodine 7%, Potassium Iodide 5%, Purified water
* Please review the disclaimer below.
