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Drug Facts
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Manufactured by:
Celeste Industries Corporation
Easton, Maryland 21601 • USA
Sani Luxe Cloth
FDA Label NDC 71489-009
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Celeste Industries Corporation for the product Sani Luxe (NDC 71489-009). 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 other, active ingredient, purpose, uses, warning, otc - when using, otc - stop use, otc - keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Ethyl alcohol (ethanol) 70%
Purpose
Antimicrobial
Uses
- For hand sanitizing to decrease bacteria on the skin
- Recommended for repeated use
Warning
For external use only.
Otc - When Using
When using this product avoid contact with eyes. In case of eye contact,
flush eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develops, or if
condition persists for more than 72 hours.
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
- Apply to hands
- Allow skin to dry without wiping
Inactive Ingredients
Water, Cocamindopropyl PG-Dimonium, Chloride Phosphate, Linear alcohol ethoxylate, Fragrance.
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