Otc - Active Ingredient
Active Ingredient(s)
Ethyl Alcohol 70% v/v. Purpose: Antiseptic
Advanced Hand Sanitizer
FDA Label NDC 79327-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Purchasing 411, Inc. for the product Advanced Hand Sanitizer (NDC 79327-001). 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 otc - active ingredient, otc - purpose, otc - keep out of reach of children, indications & usage, warnings, dosage & administration, storage and handling, inactive ingredient, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Use
- To decrease bacteria on the skin that could cause disease.
- recommended for repeated use
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.
Indications & Usage
Stop use and ask a doctor if
- Skin irritation develops
Warnings
Warnings
For external use only. Flammable. Keep away from heat or 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
Dosage & Administration
Directions
- Wet hands thoroughly with product and allow to dry without wiping
- For children under 6, use only under adult supervision
- not recommend for infants
Storage And Handling
Other information
- do not store above 105°F
- may discolor some fabrics
- harmful to wood finishes and plasics
Inactive Ingredient
Inactive ingredients water, glycerin, propylene glycol,carbomer
Package Label.Principal Display Panel
Royalty Premier
Advanced
Hand Sanitizer
Fights Germs and Bacteria
40 FL OZ (1.18 L)
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