Active Ingredients:
Ethyl Alcohol 70%
Instant Hand Sanitizer
FDA Label NDC 75416-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Liq-e, S.a. De C.v. for the product Instant Hand Sanitizer (NDC 75416-002). 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 active ingredients:, purpose, uses:, warnings:, when using this product, stop use and ask a doctor if, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antiseptic
Uses:
- For handwashing to decrease bacteria on the skin.
- Recommended for repeated use.
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 contact 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, hydrogen peroxide, fragrance, and demineralized water.
Package Labeling:
Bottle (Bottle)
* Please review the disclaimer below.
