Active Ingredient
Ethyl Alcohol 75% by volume
Dynamic Sanitizing Alcohol Wipes
FDA Label NDC 79203-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Milky Way International Trading Corp for the product Dynamic Sanitizing Alcohol Wipes (NDC 79203-002). 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, purpose, use, warning, otc - keep out of reach of children, directions, inactive ingredients, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Use
●For hand sanitizing to decrease bacteria on the skin.
●Apply topically to the skin to help prevent cross contamination.
●Not recommended for repeated use.
●Dries in seconds.
Warning
For external use only.
Flammable, Keep away from fire or flame.
When using this product do not use in or contact the eyes.
Stop use and ask a doctor if too much skin irritation or
sensitivity develops or increases.
Otc - Keep Out Of Reach Of Children
keep out of reach of children. If swallowed, contact medical help or call Poison Control immediately.
Directions
Remove lid and discard seal from container.
.Pull wipe from center of roll and thread through opening in lid.
Do not push finger through opening.
Replace lid, pull wipe up, and then out at a 45° angle. The next
wipe dispenses automatically.
.Close lid to retain moisture.
other information
.Store at room temperature 15°-30℃(59-86F).
. Lot No.Manufacture date and Expiration date can be found on
canister.
Inactive Ingredients
Water
Package Label.Principal Display Panel
1 (79203002)
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