The following Structured Product Label (SPL) was submitted to the FDA by Nimbus Eco Inc. for the product Nimbus (NDC 81240-001). 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 other, active ingredient(s), purpose, use, warnings, do not use, otc - when using, otc - stop use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
This is a hand sanitizing wipe manufactured using only the following United States Pharmacopoeia (USP) grade ingredients
Benzalkonium Chloride 0.1% Purpose: Antibacterial
Antibacterial
Decrease bacteria on the skin
For external use only.
Do not use if irritation and redness develop
When using this product avoid contact with eyes, if contact occurs, rinse thoroughly with water.
Stop use and ask a doctor if condition 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.
Open resealable label. Remove one wipe to use. Wipe hands thoroughly with product and allow to dry without wiping.
Close resealable label after use to retain moisture.
Dispose of wipe in the proper container
Do not flush down the toilet
Kill claims against: Escherichia Coli and Staphylococcus aureus
Water
Propylene Glycol
Ethyl Alcohol
Lauryl Glucoside
Phenoxyethanol
Benzalkonium Chloride
Tetrasodium EDTA
3-Iodo-2-Propynyl ButylCarbamate
2-Bromo-2-Nitropropane-1,3-Diol
Citric Acid
Fragrance N/A
Aloe Barbadensis Leaf Extract
Chamomilla Recutita Flower Extract
50 count NDC: 81240-001-50
50 Count (Newwantibac12501k5fda)
* Please review the disclaimer below.
