Active Lngredient
Alcohol 75% v/v
Locke Teddy Gel
FDA Label NDC 73928-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Kingkey Mbc Life Technology Group Co.,ltd for the product Locke Teddy (NDC 73928-001). 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 lngredient, purpose, uses, warnings, directions, other information, inactives, product label, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Anti-Bacterial
Uses
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame
Do not use
• in 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.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
Place enough product on hands to cover all surfaces. Rub hands together until dry. • Supervise children under 6 years of age when using this product to avoid swallowing
Other Information
Store between 15-30°C (59-86F)
Avoid freezing and excessively heat above 40°C (104F)
Inactives
Glycerin, Carbome, hydrogen peroxide, Purified Water USP
* Please review the disclaimer below.
