Otc - Active Ingredient
Ethyl Alcohol 70%v/v
Footspa Pedi Spray
FDA Label NDC 49283-707
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Chemco Corporation for the product Footspa Pedi (NDC 49283-707). 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, otc - purpose, uses:, warnings, flammable:, ask a doctor before use if, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Antimicrobial
Uses:
To decrease bacteria on the skin.
Warnings
• For external use only.
• Avoid contact with eyes or mucous membrane.
• Do not apply to wounds or damaged
skin with a heating pad or on a child
under 12 year of age.
Flammable:
Keep away from fire or flame.
Ask A Doctor Before Use If
If you have redness over affected area.
Otc - Stop Use
Condition persists for more than 72 hours.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help, or contact a Poison Control Center right away.
Directions:
Adults and children 12 years of age or older
• Spray two to three pumps or as
necessary to cover the affected area
not more than three to four times
daily.
Inactive Ingredient
Water (Aqua), Camphor, Polysorbate 20, Menthol, DMDM Hydantoin, Mentha Piperita (Peppermint) Oil, Eucalyptus Globulus Leaf Oil, D&C Yellow No.11(CI 47000), FD&C Blue No.1 (CI 42090).
Otc - Questions
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