Otc - Active Ingredient
Benzalkonium Chloride
Hand Sanit1zing Wipes
FDA Label NDC 81925-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhejiang Healyou Hygienics Technology Co., Ltd. for the product Hand Sanit1zing Wipes (NDC 81925-001). 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 otc - active ingredient, otc - purpose, use, warnings, otc - stop use, otc - do not use, otc - ask doctor, 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
Otc - Purpose
Antiseptic
Use
Use for hand sanitizing to reduce bacteria on the skin.
Warnings
For external use only.When using this product
Otc - Stop Use
lf irritation appears, stop use.
Otc - Do Not Use
Keep out of eyes.In case of contact, rinse eyes with water.
Otc - Ask Doctor
Consult a doctor if irritation persists more than 72 hours.
lf swallowed,get medical help or contact a Poison Control Center right away.
Otc - Keep Out Of Reach Of Children
Keep out of the reach of children, except with adult supervision.
Directions
Thoroughly wipe hands and face as desired.
Allow to dry without wiping.
Discard wipe in trash receptacle after use.Do not flush.
Inactive Ingredient
Water(Aqua),Polyhexamethylene biguanide hydrochloride,Benzalkonium Chloride,Didecyldimethylammoniumchloride,Cetylpyridinium Chloride,monohydrate,Ethylhexylglycerin,Aloe Barbadensis Leaf Extract,Glycerine.
Storage And Handling
Store at room temperature
Package Label.Principal Display Panel
Label (Label)
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