Protec Hand Sani Gel Antibacterial Gel
FDA Label NDC 67326-006
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Degasa, S.a. De C.v. for the product Protec Hand Sani Gel Antibacterial (NDC 67326-006). 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, inactive ingredients:, uses, when using this product :, directions, other information, 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%
Purpose
Antiseptic
Inactive Ingredients:
Deionized water, Carbopol, Glycerin, Triethanolamine, Aminomethylpropanol,Fragrance.
Uses
To decrease bactreria on the skin that could disease.Recommended for repeated use.
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. 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 adults supervision
- Not recommended for infants
Other Information
- Do not store above 105° F
- Harmful to wood finishes and plastic
Warnings
- For external use only: hands
- Flammable, keep away from fire or flame
Package Labeling
Label (Label)
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