Modaka Wipe Me
FDA Label NDC 77586-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Derma Innovation Company Limited for the product Modaka Wipe Me (NDC 77586-002). 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 drug facts, active ingredient, purpose, use, warnings, otc - keep out of reach of children, directions, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Benzalkonium Chloride 0.1%
Purpose
Antibacterial
Use
decrease bacteria on skin
Warnings
For external use only
Do not use if you are allergic to any of the ingredients
When using this product do not get into eyes. If contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.
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
Open the lid, tear the seal sticker, take out the wipes, adults and children 2 years and over, apply to hands
Inactive Ingredients
Water (Aqua), Phenoxyethanol, Sodium Benzoate, PEG-40 Hydrogenated Castor Oil, Citric Acid
Packaging
Image (7758600201 1)
Image (7758600201 2)
Image (7758600201 3)
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