Antiseptique Advance Strength
FDA Label NDC 72138-420

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Hubot Healthcare Llc for the product Antiseptique Advance Strength (NDC 72138-420). 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 other, active ingredient, purposes, uses, warnings, do not use, when using this product, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

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Drug Facts

Active Ingredient

Ethyl Alcohol 80% v/v

Purposes

Antiseptic handwash

Uses

Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.

Warnings

  • For external use only
  • Flammable, keep away from heat or flame.

Do Not Use

  • In eyes | on children less than 2 months old | on open skin wounds

When Using This Product

  • Keep out of eyes, ears and mouth. In case of contact with eyes, rinse eyes thoroughly with water.

Otc - Stop Use

Stop use and ask a doctor if skin irritation or rash occurs. There may be signs of a serious conditions.

Otc - Keep Out Of Reach Of Children

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

  • Place enough product on hands to cover all surfaces. Rub hands together until dry. Supervise children under 6 years of age when using this product to avoid swallowing.

Other Information

  • Store between 15-30°C (59-86°F), Avoid freezing and excessive heat above 40°C (104°F)

Inactive Ingredients

Purified Water USP, Glycerin, Hydrogen Peroxide

Principal Display Panel - 59 Ml Bottle Label

ANTISEPTIQUE+
ADVANCED STRENGTH
sanitizer mist

Alcohol Antiseptic 80%
Topical Non-sterile Solution

2 FL. OZ. (59 ML)

Principal Display Panel (59 ML Bottle Label)

Principal Display Panel (59 ML Bottle Label)

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