Mynt. Hand Sanitizing Wipes
FDA Label NDC 79006-101
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Sharp International Distributors Inc. for the product Mynt. Hand Sanitizing Wipes (NDC 79006-101). 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, uses, warnings, keep out of reach of children., directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Alcohol, 75% v/v
Purpose
Antiseptic
Uses
• Hand sanitizer to help reduce bacteria that could cause disease
• Recommended for repeated use
Warnings
Flammable, keep away from fire or flame
For external use only
Do not use with electrocautery procedures.
When using product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if irritation and redness develop and persists more than 72 hours
Keep Out Of Reach Of Children.
If accidentally swallowed, get medical help or contact a Poison Control Center right away
Directions
• Apply to skin as needed
• Discard after single use
Other Information
▪ Protect from freezing and avoid excessive heat
Inactive Ingredients
Water (Aqua), Propylene Glycol, Phenoxyethanol, PEG-40 Hydrogenated Castor Oil, PEG-12 Dimethicone, Prunus Amygdalus Dulcis Oil, Dissodium ETDA
Packaging
Image (7900610110)
Image (7900610120)
Image (7900610140)
Image (7900610150)
Image (7900610180)
Image (7900610115)
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