Hand Sanitizer
FDA Label NDC 73742-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Golden Applexx Co., Inc. for the product Hand Sanitizer (NDC 73742-101). 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 ingredients:, purpose:, uses:, warning:, directions:, inactive ingredients:, packaging, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredients:
Ethyl Alcohol 62%
Purpose:
Antiseptic
Uses:
• hand sanitizer to decrease bacteria on the skin
• recommended for repeated use
• for use when soap and water are not available
Warning:
For External Use Only
Do not apply in or around eyes. In case of contact, rinse eyes thoroughly with water. Avoid contact with broken skin. Do not inhale or ingest. Stop use and ask a doctor if irritation and redness develop and last for more than 72 hours. Get immediate medical help if swallowed.
Flammable, keep away from fire or flame.
Directions:
• wet hands thoroughly with product and allow to dry without wiping
• supervise children under 6 years of age when using this product to avoid swallowing
Inactive Ingredients:
Water, Glycerin, Essential Oils
Packaging
Hndstzr (Hndsntzr1)
* Please review the disclaimer below.
