Active Ingredient(S)
Benzalkoniu m Chlloridle O.13%
Wipes
FDA Label NDC 77909-010
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Huihao Medical Technology (zhejiang) Co., Ltd for the product Wipes (NDC 77909-010). 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), use, warnings, do not use, 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
Use
for hand sanitizing to decrease bacteria on skin
safe for repeated use
Warnings
For exter1nal use onlly
Do Not Use
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Otc - When Using
When using this p1rodlu1ct avoid contact with eyes. If in1e yes, flush thoroughly with water
Otc - Stop Use
Discontinue use and contact a doctor if irritation and redness develop and conditions persist for more than 72hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away
Directions
peel back label
remove and un1fold wipes
wipe hands thoroughly for approximately 30seconds
dispose of used wipes in trash, do not flush.
Other Information
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Inactive Ingredients
Glycerin, Aloe Vera, Vitamin E, Purified Water
* Please review the disclaimer below.
