Active Ingredient(S)
Ethyl alcohol 65% Purpose: Antiseptic
Hand Sanitizer
FDA Label NDC 76861-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Liangxin Refinement Chemical Co.,ltd for the product Hand Sanitizer (NDC 76861-002). 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 active ingredient(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic, Hand Sanitizer
Use
For hand washing to decrease bacteria on the skin
Warnings
For external use only. Flammable. Keep away from heat or flame
Otc - When Using
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.
Otc - Stop Use
stop use and ask a doctor if
irritation and redness develop
condition persists for more 72hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
wet hands thoroughly with product and allow to dry without wiping
Other Information
Store in a cool,dry place
Inactive Ingredients
water,aloe vera extract,fragrance,carbomer
Package Label - Principal Display Panel
60 mL NDC: 76861-002-01
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