Ripclear Antiseptic Hand Sanitizer
FDA Label NDC 80555-001
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Rip Clear Llc for the product Ripclear Antiseptic Hand Sanitizer (NDC 80555-001). 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 drug facts, active ingredient, purpose, indications & usage, warnings, otc - keep out of reach of children, other information, inactive ingredients, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient
Isopropyl alcohol 75% v/v
Purpose
Antiseptic
Indications & Usage
Uses • hand sanitizer to decrease bacteria on the skin • recommended for repeated use • for use when soap and water are not available
Warnings
Flammable, keep away from fire/flame
For external use only
Do not use • in children less than 2 months of age • on open skin wounds
When using this product • do not get into eyes. In case of contact, rinse eyes thoroughly with water
Stop use and ask a doctor if • irritation and redness develop • condition persists for more than 72 hours
Otc - Keep Out Of Reach Of Children
Keep out of reach of children. If swallowed get a medical help or contact a Poison Control Center right away.
Other Information
• store between 59-86°F (15-30°C) • avoid freezing and excessive heat above 104°F (40°C)
Inactive Ingredients
acrylates/c-10-30 alkyl acrylate crosspolymer, aloe vera leaf juice, aminomethylpropanol, FD&C Blue #1, FD&C Red #40, fragrance, glycerin, propylene glycol, propylparaben, water
Packaging
Untitled (80555 001)
* Please review the disclaimer below.
