Active Ingredient(S)
Isopropyl Alcohol 70%
Sanitizing Wipe
FDA Label NDC 72766-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Yangzhou Suxiang Medical Instrument Co., Ltd. for the product Sanitizing Wipe (NDC 72766-004). 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, do not use, otc - when using, otc - stop use, 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
Purpose
Antiseptic
Use
For External Use Only
Warnings
For external use only.
Flammable. Keep away from fire or flame
Do Not Use
On open skin wounds
Otc - When Using
Do not use in or near the eyes. In case of contact with eyes flush thoroughly with water.
Use wipes only on unbroken, intact skin
Do not ingest
Otc - Stop Use
If skin irritation or redness develops
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
Wipe hands thoroughly, let skin dry and discard
Keep out of reach of children. Children under 6 years of age use only under adult supervision
Not recommended for infants
Do not store above 105°F
Other Information
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Inactive Ingredients
Water
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