Progel360 Hand Sanitizer
FDA Label NDC 78567-070
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Steltz Pharmacy, Inc. D/b/a Consolidated Medical Supply for the product Progel360 Hand Sanitizer (NDC 78567-070). 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, use(s), warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl Alcohol 70%
Purpose
Antiseptic
Use(S)
Hand sanitizer to help reduce bacteria that potentially can cause disease. For use when soap and water are not available.
Warnings
For external use only. Flammable. Keep away from heat or flame.
When using this product keep out of eyes, ears, and mouth. In case of contact with eyes, rinse eyes thoroughly with water.
Stop use and ask a doctor if irritation or rash occurs. These may be signs of a serious condition.
Otc - Keep Out Of Reach Of Children
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
• Avoid contact with broken skin
• Do not ingest, inhale, or inject
Inactive Ingredients
Purified Water, Hydrogen Peroxide, Carbomer 940, Triethanolamine, Polyethylene Glycol, Glycerin
Packaging
Image (78567070 02)
Image (78567070 16)
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