Katra Hand Sanitizer
FDA Label NDC 81103-002

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

Structured Product Label

The following Structured Product Label (SPL) was submitted to the FDA by Ths Cosmetic Eood for the product Katra Hand Sanitizer (NDC 81103-002). 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 drug facts, active ingredient:, purpose:, uses:, warning:, otc - keep out of reach of children, directions:, other information:, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.

Label Section Quick Index

→ Drug Facts

→ Active Ingredient:

→ Purpose:

→ Uses:

→ Warning:

→ Otc - Keep Out Of Reach Of Children

→ Directions:

→ Other Information:

→ Inactive Ingredients:

→ Packaging

Drug Facts

Active Ingredient:

Ethyl Alcohol 75% v/v

Purpose:

Antiseptic

Uses:

To decrease germs on the skin. Hand Sanitizer to help reduce germs that potentially can cause diseases.

Warning:

FOR EXTERNAL USE ONLY: HANDS
Flammable. Keep away from fire, heat or flame.

Do not use near eyes. In case of contact, rinse eyes thoroughly with water. On children less than 2 months of age. On open skin wounds.
Stop use and ask a doctor if redness or irritation develop and persist for more than 72 hours. If swallowed - get medical help or contact a Poison Control Center right away.