Otc - Active Ingredient
Allantoin 0.5%
Kenaf Wet Wipe Kids Liquid
FDA Label NDC 72944-0002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Medicell Bio Co., Ltd. for the product Kenaf Wet Wipe Kids (NDC 72944-0002). 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 otc - active ingredient, inactive ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, 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
Inactive Ingredient
Water, etc
Otc - Purpose
wet tissue
Otc - Keep Out Of Reach Of Children
keep out of reach of the children
Indications & Usage
Apply to skin and wipe
Warnings
1. For external use only.
1) Do not use over the wound and irritated skin with eczema or infections
2) Discontinue using the product if signs of irritations and/or rashes occur and seek professional medical help
2. Keep the cover closed tight after use
3. Do not put the left over contents back into the container to avoid deterioration
1) Avoid contact with eyes
2) Keep out of reach of children
3) Store in a cool and dry place, away from direct sun light
Dosage & Administration
for external use only
Package Label.Principal Display Panel
Label (Product)
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