Hand Sanitizer
FDA Label NDC 74341-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Newacme Llc for the product Hand Sanitizer (NDC 74341-004). 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 ingredients, purpose, uses:, warnings:, when using this product, stop use and ask a doctor, 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 Ingredients
Ethyl Alcohol 70% v/v
Purpose
Antiseptic
Uses:
For Hand Sanitizing.
Warnings:
For external use only-hands.
Flammable: Keep away from heat and flame.
When Using This Product
- Keep out of eyes. In case of contact with eyes, flush thoroughly with water.
- Avoid contact with broken skin.
- Do not inhale or ingest.
Stop Use And Ask A Doctor
If skin irritation develops.
Keep Out Of Reach Of Children.
If swallowed, get medical help or call a Poison Control Center right away.
Directions:
Wet hands thoroughly with product and allow to dry without wiping
- For children under 6 use only under adult Supervision.
- Not recommended for infants.
Other Information:
Do not store above 105°F.
- May discolor some fabrics.
- Harmful to wood finishes and plastics.
Inactive Ingredients:
Carbomer, Fragrance, Glycerin, Propylene Glycol, Tocopheryl Acetate, Triethanolamine, Water.
Package Labeling:1000Ml
Bottle (Bottle)
Package Labeling:2000Ml
Bottle2 (Bottle2)
Package Labeling:3.780Ml
Bottle3 (Bottle3)
* Please review the disclaimer below.
