Kenda Care Instant Hand Sanitizer
FDA Label NDC 76038-404

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Micro Connection Enterprises Inc for the product Kenda Care Instant Hand Sanitizer (NDC 76038-404). 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, use, warnings, otc - keep out of reach of children, directions, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

Active Ingredient

ETHYL ALCOHOL 70% W/V

Purpose

ANTIMICROBIAL

Use

Hand sanitizer to help reduce bacteria on the skin that could cause disease.

Warnings

For external use only. Flammable. Keep away from heat and flame. Do not inhale or ingest. Keep out of eyes, ears, and mouth. If eye contact occurs, flush thoroughly with water and seek medical advice. Avoid contact with broken skin. Not for use on infants. Stop use and ask a doctor if irritation, rash, or redness occurs. These may be signs of a serious condition.

Otc - Keep Out Of Reach Of Children

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

Directions

  • Dispense directly on hands and rub in thoroughly.
  • Children under 6 should be helped and supervised.

Other Information

Store between 15°C and 37°C (59°F and 99°F). Avoid freezing. Avoid excessive heat above 40°C (104°F).

Inactive Ingredients

Water, Glycerin, Aminomethyl Propanol, Acrylates/C10-30 Alkyl Acrylate Crosspolymer

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