Active Ingredient(S)
Ethyl Alcohol 62% Purpose Antiseptic
Hand Sanitizer
FDA Label NDC 74034-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sichuan Rejoy Essence Biotechnology Co., Ltd for the product Hand Sanitizer (NDC 74034-006). 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, uses, warnings, when using this product, otc - when using, otc - stop use, 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
Purpose Antiseptic
Uses
Decreases Bacteria On Hands
Warnings
For External Use Only
When Using This Product
When using this product,do not use in or near the eyes.
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
/
Keep Out Of Reach Of Children
If swallowed,get medical help or contact a Poison
Control Center immediately.
Directions
Squeeze onto hands and rub hands
together briskly until dry. Do Not Store Above
110°F Non-staining,may discolor certain fabrics
Other Information
Do Not Store Above
110°F Non-staining,may discolor certain fabrics
Inactive Ingredients
Deionized Water,Carbomer,Triethanolamine,
Aloe Barbadensis ,Ethanol,Glycerol,
Propylene Glycol,Vitamin E.
Package Label - Principal Display Panel
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