Active Ingredient
Ethyl Alcohol 75%
Wet Wipe
FDA Label NDC 76906-006
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 Beitao Hygienic Products Co., Ltd. for the product Wet Wipe (NDC 76906-006). 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, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptice Handwash
Use
For hand sanitizing to decrease bacteria on the skin.
Do not recommended for repeated use.
Warning
For external use only
When using this product,
Do not use in or near eyes. In case of touch, rinse with running water immediately.
Avoid moisture evaporation, cover it at once after use.
Can not throw into toilet
Stop use and ask a doctor if too much irritation or sensitivity develops or increases.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Directions
Take wipe and rub thoroughly over all surfaces of both hands
Rub hands together briskly to dry
Dispose of Wipe
Inactive Ingredients
Aqua,Glycerin,Aloe Barbadensis Leaf Juice.
Other Information
Do not store above 110F
May discolor some fabrics
Package Label.Principal Display Panel
80PCS NDC 76906-006-01
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