Active Ingredient
Ethyl Alcohol 66.5%
Redicare Antiseptic Wipes
FDA Label NDC 71105-311
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Redicare Llc for the product Redicare Antiseptic Wipes (NDC 71105-311). 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, purpose, uses, warnings, do not use, stop use and ask a doctor if, 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
Antiseptic
Uses
- for handwashing to decrease bacteria on skin whenever soap and water are not readily available
Warnings
For external use only.
Flammable, keep away from fire or flame
Do Not Use
in the eyes. If this happens, rinse thoroughly with water.
Stop Use And Ask A Doctor If
- irritation or redness develops and persists for more than 72 hours
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
- Tear open packet, remove towelette
- wet hands and wrists thoroughly for 15 seconds and discard
- supervise children under 6 years of age
Inactive Ingredients
Aloe vera, fragrance, purified water, triethanolamine
* Please review the disclaimer below.
