Nnp Hand Sanitizer
FDA Label NDC 78462-007
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Nevada Zona Libre, S.a. for the product Nnp Hand Sanitizer (NDC 78462-007). 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, when using this product, stop use and ask a doctor if, 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
Active Ingredient
Alcohol 69.99% v/v
Purpose
Antiseptic
Uses
- To decrease bacteria on the skin that could cause disease.
- Recommended for repeated use.
Warnings
- For External Use Only
- Flammable
- Keep Away From Fire or Flame
When Using This Product
- Keep out of eyes.
- In case of contact with eyes, flush thoroughly with water
- Avoid contact with wounded skin
- Do not inhale or ingest.
Stop Use And Ask A Doctor If
- Irritation or redness develops
- Condition persists for more than 72 hourse.
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away
Directions
- Pleace enough product on hands to cover all surfaces.
- Rub hands together until dry.
- Supervise children under 6 years of age when using this product to avoid swallowing.
Other Information
- Do not store above 105°F
- May discolor some fabrics
- Harmful to wood finishes and plastics.
Inactive Ingredients
Water, Propylene, Glycol, Glycerin, Carbomer, Triethanolamine, Tocopheryl Acetate, Aloe Barbadensis Extract.
Package Labeling: 60Ml
Label (Label)
Package Labeling: 300Ml
Label2 (Label2)
Package Labeling: 1000Ml
Bottle (Bottle)
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