Active Ingredients
Ethanol 75 ± 5% (V/V)
Vivacious Instant Hand Sanitizer
FDA Label NDC 77572-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Global 1 Wholesale Merchant Services, Inc. for the product Vivacious Instant Hand Sanitizer (NDC 77572-001). 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 ingredients, purpose, use, warnings, do not use, 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
Purpose
Antiseptic
Use
To reduce bacteria on hand
Warnings
For External Use Only
Flammable. Keep away from Heat or Flame
Do Not Use
In children less than 2 months of age
On open skin wounds
Otc - When Using
Keep out of eyes, ears, and mouth. In case of contact with eyes, rinse thoroughly with water
Otc - Stop Use
Stop use and ask a doctorif irritation or rash occur
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
Place enough amount of product on hands to cover all surface.
Rub hands until dry.
Supervise children under 6 years old when using this product to avoid swallowing.
Other Information
Store between 15 - 30°C (59 - 86°F)
Avoid Freezing and Excessive Heat above 40°C (104°F)
Inactive Ingredients
Aqua (Water), Carbomer, Glycerol, Triethanolamine
Package Label.Principal Display Panel
60 mL - NDC 77572-001-35
Label-60ml (Label 60ml)
500 mL - NDC 77572-001-40
Label-500ml (Label 500ml)
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