Active Ingredients
Iodine 2.0%
Sodium Iodide 2.4%
Iodine Tincture
FDA Label NDC 65055-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Laboratorios Jaloma, S.a. De C.v. for the product Iodine Tincture (NDC 65055-101). 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 ingredients, purpose, uses, warnings, otc - do not use, otc - ask doctor, otc - stop use, otc - 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
Antiseptic
Uses
First aid to help prevent infection in *minor cuts *scrapes *burns
Warnings
Warnings
For external use only
Otc - Do Not Use
Do not use in the eyes or apply over large areas of
the body
Do not use longer than 1 week, unless directed by a
doctor
Otc - Ask Doctor
Consult a doctor in case of * deep or puncture
wounds * animal bites * serious burns
Otc - Stop Use
Stop use and consult a doctor if the condition
persists or gets worse
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children. In case of
accidental ingestion, seek professional assistance
or contact a Poison Control Center immediately.
Dosage & Administration
Directions clean the affected area * apply a
small amount of this product on the area 1 to 3
times daily * may be covered with a sterile bandage
Inactive Ingredients
alcohol, water
Otc - Questions
Questions
(33) 3617 5010 (In Guadalajara, Jal. Mexico)
* Please review the disclaimer below.
