Iodine Tincture Rojo
FDA Label NDC 70242-110

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Dannso Corp./d.b.a. Essential Products for the product Iodine Tincture Rojo (NDC 70242-110). 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, use, warnings, inactive ingredient, stop use and ask a doctor, 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 Ingredients

Iodine 2%

Purpose

First aid antiseptic

Use

First aid to help prevent sking infection in

  • minor cuts
  • scrapes
  • burns

Warnings

Warnings

For external use only. Avoid contact with eyes or with mucous membrane. Keep out of the reach of children. Children under 2 years please consult a physician. Do not apply on irritated skin, in or near eyes or mocuos memebranes, on wounds or damamged skin, or if it causes allergic reaction. In case of accidental ingestion, seek professional assistance or contact Poison Control Center immedialately.


Inactive Ingredient

Deionized Water, Isopropyl Alcohol, Sodium Iodine.

Stop Use And Ask A Doctor

Redness, Irritation, Swelling, Pain persists, or increases, infection, Rash, or irritation occurs.

Keep Out Of Reach Of Children

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

Directions

  • Clean the affected area and dry thorougkyapply.
  • Apply a thin layer 1 to 3 times daily
  • Do not cover with bandage

Principal Display Panel

IODO ROJO

Label (Iodorojo)

Label (Iodorojo)

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