Eco Sanitizer Gel
FDA Label NDC 80731-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by 0966452 B.c. Ltd. for the product Eco Sanitizer Gel (NDC 80731-002). 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 otc - purpose, indications & usage, dosage & administration, otc - active ingredient, inactive ingredient, warnings, otc - keep out of reach of children, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Otc - Purpose

Purpose: Antiseptic

Indications & Usage

Use: Hand sanitizer to help reduce bacteria on skin

Dosage & Administration

Directions for Use: Supervise children when they use this product. For occasional and personal domestic use. Rub thoroughly into hands for at least 30 seconds. Allow to dry.

Otc - Active Ingredient

Medicinal Ingredients: Ethyl Alcohol* (70% v/v).

Inactive Ingredient

Ingredients: Aqua, Glycerin,* Hydroxypropylcellulose*. *Plant based ingredient.

Warnings

Warning: For external use only. Keep out of reach of children. Flammable. Keep away from open flame and sources of heat. Avoid contact with eyes. Should this occur, flush eyes with water. If irritation develops, discontinue use and contact a health care practitioner. Store between 15°C/59°F and 30°C/86°F.

Contraindications: Do not use on children/infants less than 2 years of age (unless directed by a health care practitioner).

Otc - Keep Out Of Reach Of Children

Keep out of reach of children.

Packaging

Image (8073100203lb)

Image (8073100203lb)

* Please review the disclaimer below.