Doctor Inks Hand Sanitizer Liquid
FDA Label NDC 71884-201

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Enviro Specialty Chemicals Inc for the product Doctor Inks Hand Sanitizer (NDC 71884-201). 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 drug facts, active ingredient:, purpose:, uses:, warnings:, otc - keep out of reach of children, directions:, inactive ingredients:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Drug Facts

Active Ingredient:

Benzalkonium Chloride 0.13%

Purpose:

Antiseptic, Hand & Skin Sanitizer

Uses:

Hand Sanitizer to help decrease bacteria on the skin - Recommended for repeated use.

Warnings:

Do not freeze. For external use only. Do not use in ears, eyes or mouth.

  • When using this product, avoid contact with the eyes. In case of contact, flush eyes with water.
  • Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.
  • Children should be supervised when using this product.

Directions:

Apply liberally to the palms of the hands. Rub into skin until dry. Recommended for repeat use.

Inactive Ingredients:

Aloe Barbadensis leaf extract, Aqua, Citric Acid, Laureth-4, Phenoxyethanol, Triethoxysilylpropyl Steardimonium chloride.

Questions?

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Packaging

Sanitizerfoam (71884 201 04)

Sanitizerfoam (71884 201 04)

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