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Other information
- store between 15-30°C (59-86°F)
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Clearguard Hand Sanitizer
FDA Label NDC 80996-002
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Evp International, Llc for the product Clearguard Hand Sanitizer (NDC 80996-002). 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, otc - active ingredient, otc - purpose, indications & usage, warnings, 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
Otc - Active Ingredient
Active ingredient
Alcohol 70% v/v
Otc - Purpose
Purpose
Antiseptic
Indications & Usage
Uses
to help reduce bacteria on skin
Warnings
Warnings
For external use only
Flammable, keep away from heat or flame.
Otc - When Using
When using this product keep away from eyes. In case of eye contact, rinse eyes with water.
Otc - Stop Use
Stop use and ask a doctor if irritation or redness develop or last more than 72 hours.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed, get medial help or contact a Poison Control Center immediately.
Dosage & Administration
Directions
- apply liberally to hands to cover all surfaces
- rub hands together until dry
- supervise children under 6 years old
- not recommended for infants
Inactive Ingredient
Inactive ingredients
glycerin, hydrogen peroxide, purified water, acrylates/C10-30 alkyl acrylate crosspolymer, aminomethyl propanol, lauryl lactate, fragrance
Package Label.Principal Display Panel
ClearGuard
Hand Sanitizer
Alcohol Based
2 FL OZ (59 mL)
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