Active Ingredient(S)
Alcohol 62%
Hand Sanitizer Liquid
FDA Label NDC 85279-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangdong Bangze Medicine Co., Ltd for the product Hand Sanitizer (NDC 85279-003). 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(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antibacterial
Use
Hand Sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
Flammable. Keep away from fire or flame. For extermnal use only.
Do Not Use
Do not use it near eye area. In case of contact, rinse eyes thoroughly with water.
Otc - When Using
When using this product keep out of eyes, In case of contact with eyes, rinse eyes thoroughly with water.
Otc - Stop Use
Stop use and ask a doctor if initation or rash appears and lasts
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
■Apply into hand and thoroughly spreadon both hands, rub until dry.
■Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
■Store between 15- 30°C ( 59 - 86°F )
■Avoid freezing and excessive heat above 40°C (104°F )
Inactive Ingredients
Aqua/Water, Glycerin, Fragrance
Package Label - Principal Display Panel
001 (Label1)
002 (Label2)
003 (Label3)
004 (Label4)
005 (Label5)
006 (Label6)
007 (Label7)
008 (Label8)
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