Orbit Hand Sanitizer
FDA Label NDC 78752-698
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Orbit Capital Llc for the product Orbit Hand Sanitizer (NDC 78752-698). 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, inactive ingredients, uses, other information, questions?, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Isopropyl Alcohol (70%)
Purpose
Antiseptic
Inactive Ingredients
Glycerine, DM Sterile water, Carbomer, Vitamin E, Aloe Extract, H2O2, Triethanolamine
Uses
▪ For hand-washing to decrease bacteria on the skin.
▪ Recommended for repeated use.
▪ Avoid contact with broken skin.
▪ Do not inhale or ingest.
Other Information
Do not store above 105°F
May discolor some fabrics
Harmful to wood finishes and plastics
Questions?
+1(877)793-8998
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.
Stop use and ask a doctor if skin irritates develops.
Directions
Wet hands thoroughly with product and allow to dry without wiping.
For children under 6 years, use only under adult supervision.
Not a recommendation for infants
Packaging
Image (78752698 01)
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