Otc - Active Ingredient
BENZALKONIUM CHLORIDE
Instant Hand Sanitizeing Wipe
FDA Label NDC 96292-001
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 Yayun Biotechnology Co., Ltd. for the product Instant Hand Sanitizeing Wipe (NDC 96292-001). 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, uses, warnings, otc - do not use, otc - ask doctor, 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
Otc - Purpose
Antiseptic
Uses
For handwashing to decrease bacteria on the skin.
Warnings
For external use only.
Otc - Do Not Use
Do not use in or contactwith eyes.
Otc - Ask Doctor
Discontinue use if irritation and rednessdevelop.if condition porsists more than 72 hours,consult a doctor.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision. if swallowed,get medical help or contact a Poison Control Center right away.
Directions
Tear open packet. Unfold and apply wipe thoroughly onto hands.
Discard after single use. No rinsing required. Dispose of used wipes in trash receptacle. Do not flush.
Other Information
Store at 59-86°F (15-30°C).
Inactive Ingredient
POLYAMINOPROPYL BIGUANIDE
ETHYLHEXYLGLYCERIN
DECYL GLUCOSIDE
PHENOXYETHANOL
POLYSORBATE 20
WATER
Package Label.Principal Display Panel
Label (Label)
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