Accuban Gel
FDA Label NDC 80620-110

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Tel Group Llc for the product Accuban Gel (NDC 80620-110). 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 other, active ingredient, purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Other

Drug Facts

Active Ingredient

Ethyl Alcohol 70% v/v ........ antimicrobial

Purpose

Antiseptic, Hand Sanitizer

Use

Hand Sanitizer to reduce bacteria on the skin.

Warnings

Flammable. Avoid contact with open flames.

Otc - When Using

Avoid contact with eyes.  If contact occurs flush immediately with plenty of water.

External use only

Otc - Stop Use

Stop use immediately if redness or irritation occurs and lasts.

Otc - Keep Out Of Reach Of Children

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

Directions

  • Wet hands thoroughly for at lest 15 seconds
  • Allow to air dry
  • Supervise use by children

Other Information

Store below 105F (41C)

May be damaging or discoloring to certain fabrics, wood, plastics and decorative finishes.

Inactive Ingredients

Water, Isopropyl Alcohol, PEG-6 (and) AMP Acrylates/Vinyl Isodecanoate Crosspolymer, Isononyl Isononanoate, Isopropyl Myristate

Package Label - Principal Display Panel

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