Active Ingredient
Alcohol 65%
Gelrite
FDA Label NDC 61924-106
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Dermarite Industries, Llc for the product Gelrite (NDC 61924-106). 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 ingredient, purpose, uses, warnings, directions, other information, inactive ingredients, questions?, 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 skin.
- Recommended for repeated use.
Warnings
For external use only.
Flammable. Keep away from heat and flame.
Avoid contact with eyes. In case of contact, flush thoroughly with water.
Stop use and ask a doctor if skin irritation develops.
.
Directions
- Wet hands thoroughly with product and allow to dry without wiping.
- Children under six should be supervised while using this product.
Other Information
- Do not store above 105°F
- May discolor some fabrics or surfaces
- You may report a serious adverse event to DermaRite Industries, PO Box 7209, North Bergen, NJ 07047
Inactive Ingredients
Water, Propylene Glycol, Carbomer, Polysorbate 20, Fragrance, t-Butanol, Triethanolamine, Tocopherol Acetate, Sodium Isostearoyl Lactate, Denatonium Benzoate
Questions?
Call 1-800-337-6296 Mon-Fri 9AM-5PM EST.
Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away
* Please review the disclaimer below.
