Sunmark Iodides Tincture Liquid
FDA Label NDC 49348-711

Full FDA labeling including Indications, Dosage, Usage, and Precautions

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Strategic Sourcing Services Llc for the product Sunmark Iodides Tincture (NDC 49348-711). 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, use, warnings, when using this product, stop use and consult doctor if the, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Ethyl Alcohol 48%

Purpose

First Aid Antiseptic                        

Use

first aid to help prevent infection in minor cuts, scrapes and burns.

Warnings

For external use only

When Using This Product

do not use in the eyes or apply over large areas of the body. In case of deep or puncture wounds, animal bites, or serious burns, consult a doctor.

Stop Use And Consult Doctor If The

condition persists or gets worse. Do not use this product for longer than 1 week unless directed by a doctor.

Keep Out Of Reach Of Children.

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

Directions

  • Clean the affected area.
  • apply a small amount on the area 1 to 3 times daily.
  • may be covered with sterile bandage.
  • if bandaged, let dry first.

Other Information

store at room temperature

Inactive Ingredients

ammonium hydroxide, iodine, potassium iodide, and purified water

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Label

Label (L120792074 Sm Iodides Tincture Web)

Label (L120792074 Sm Iodides Tincture Web)

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