Benemax Advanced Hand Sanitizer
FDA Label NDC 73700-004

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Nugale Pharmaceutical Inc for the product Benemax Advanced Hand Sanitizer (NDC 73700-004). 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, warnings, directions, uses, keep out of reach of children, inactive ingredient, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Purpose

Antiseptic

Warnings

For external use only. Flammable. Keep away from heat or flame.

Do not use
• on children less than 2 months of age
• 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.

Stop use and ask a doctor if irritation or rash occurs. These may
be signs of a serious condition.

Directions

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

Uses

Antiseptic and Hand Sanitizer to help reduce bacteria that may cause disease. For use when soap & water are unavailable.

Keep Out Of Reach Of Children

If swallowed, get medical help or contact a Poison Control Center right away at 1-800-222-1222.

Inactive Ingredient

Water

Other Information

Store between 15 °C and 30 °C. Avoid freezing and excessive heat above 400 °C (104 °F)

Product Label

Image Description (Updatedimage 2)

Image Description (Updatedimage 2)

* Please review the disclaimer below.