Active Ingredient
lsopropyl Alcohol 70%.........Antiseptic
Hand Sanitizer Wipes Cloth
FDA Label NDC 54860-494
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Lantern Scicence Co.,ltd. for the product Hand Sanitizer Wipes (NDC 54860-494). 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, uses, warning, directions, keep out of reach of children, other information, inactive ingredients, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Uses
Hand sanitizing to decrease bacteria on skin.
Recommended for repeated use.
Warning
For external use only.
Flammable, keep away from fire or flame.
Do not use this product in or near eyes. lf contact occursrinse thoroughly with water.
Keep out of reach of children unless under adult supervision.
Discontinue use if skin irritation and redness develop.
If condition persists for more than 72 hoursconsult a physician.
Directions
Tear open package and unfold wipe.
Thoroughly wipe hands, fingers and wrists.
Be sure to use entire wipe for approximately 20 seconds.
No rinsing or toweling is required.
Discard after single use. Do not flush.
Keep Out Of Reach Of Children
Keep out of reach of children unless under adult supervision..Discontinue use if skin irritation and redness develop.
Other Information
Store below 104°F(40°)
May discolor some fabrics
Inactive Ingredients
Purified Water (Aqua), Glycerine.Hydrogen Peroxide.
Dosage & Administration
Packing
* Please review the disclaimer below.
