Active Ingredient(S)
70% Alcohol
Hand Sanitizer
FDA Label NDC 79931-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Steel Supplements, Inc. for the product Hand Sanitizer (NDC 79931-001). 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 active ingredient(s), purpose, use, warnings, otc - when using, otc - stop use, otc - keep out of reach of children, directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antimicrobial
Use
To decrease bacteria on the skin that could cause disease. Recommended for repeated use.
Warnings
- For external use only.
- Flammable.
- May discolor some fabrics.
- Harmful to wood finishes and plastics.
Otc - When Using
Keep out of eyes, in case of contact with eyes, flush thoroughly with water. Do not inhale or ingest. Avoid contact with broken skin.
Otc - Stop Use
Stop use and ask a doctor if skin irritation develops.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. In case of accidental ingestion, seek medical help or contact a Poison Control Center immediately.
Directions
- Wet hands thoroughly with product and allow to dry without wiping.
- For children under 6 years of age only under adult supervision.
Other Information
- Store between 15-30℃(59-86℉).
- Avoid freezing and excessive heat above 40℃(104℉).
Inactive Ingredients
Water, Glycerin, Tocopheryl Acetate, Vanilla Bean Aromatica.
Package Label - Principal Display Panel
30 mL in 1 BOTTLE, NDC: 79931-001-01
30ml Label (30ml)
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