Antiseptic Solution
FDA Label NDC 66977-032

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Mpm Medical, Llc for the product Antiseptic (NDC 66977-032). 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, directions, other information, inactive ingredients, package label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

Benzethonium chloride 0.1%

Purpose

Antiseptic

Uses

  • To clean superficial wounds
  • For washing small superfical wounds
  • Aids in removal of foreign material such as dirt and debris
  • First-aid product

Warnings

For external use only.

This product is not for use on wild or domestic animal bites. If you have an animal bite, consult your physician immediately.

Do not use this product for more than 10 days. If condition worsens or persists, see your physician.

Do not bandage tightly.

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

Directions

Apply to affected area.

Adults and children 2 years of age or older: Spray on the affected area up to 3 times per day.

May be covered with a sterile bandage, if bandaged let dry first.

Children under 2 years: Consult a physician prior to use.

Other Information

Store at room temperature

Inactive Ingredients

Deionized water, disodium EDTA, glycerin, methylparaben, phosphoric acid, polyethylene-polypropylene glycol, sodium hydroxide

Package Label

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