Medical Sanitizer
FDA Label NDC 80101-102
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Cedar Medical Llc for the product Medical Sanitizer (NDC 80101-102). 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(s), purpose, use(s), warnings, otc - 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(S)
Alcohol 70% v/v
Purpose
Antiseptic
Use(S)
• Health care personnel hand rub to help reduce bacteria that potentially can cause disease
Warnings
For external use only. Flammable. Keep away from heat or flame
Do not use
• On children less than 2 months of age
• On open skin wound
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water.
Stop use and ask a doctor if irritation occurs. These may be signs of a serious disease.
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
• Place enough product on hands to cover all surfaces. Rub hands together until dry.
• Supervise children under 6 years of age when using the product to avoid swallowing
Other Information
• Store between 15-30C (59-86F)
• Avoid freezing and excessive heat above 40C (104F)
Packaging
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