Nimbus
- Dosage form
- CLOTH
- Labeler
- Nimbus Eco Inc.
- Label updated
- 2022-01-13
- Retrieved
- 2026-09-07
- Active ingredients
- BENZALKONIUM CHLORIDE
Label information
This is a hand sanitizing wipe manufactured using only the following United States Pharmacopoeia (USP) grade ingredients
- Benzalkonium Chloride (USP grade) (0.12%, volume/volume (v/v))
- Water
c. Propylene Glycol
d. Ethyl Alcohol
e. Lauryl Glucoside
f. Phenoxyethanol
g. Tetrasodium EDTA
h. 3-Iodo-2-Propynyl ButylCarbamate
i. 2-Bromo-2-Nitropropane-1,3-Diol
j. Citric Acid
k. Fragrance
l. Aloe Barbadensis Leaf Extract
m. Chamomilla Recutita Flower Extract
Active Ingredient(s)
Benzalkonium Chloride 0.1% Purpose: Antibacterial
Purpose
Antibacterial
Use
Decrease bacteria on the skin
Warnings
For external use only.
Do not use
Do not use if irritation and redness develop
Label information
When using this product avoid contact with eyes, if contact occurs, rinse thoroughly with water.
Label information
Stop use and ask a doctor if condition persists for more than 72 hours.
Label information
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.
Directions
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.
Other information
Dispose of wipe in the proper container
Do not flush down the toilet
Kill claims against: Escherichia Coli and Staphylococcus aureus
Inactive ingredients
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
Package Label - Principal Display Panel
50 count NDC: 81240-001-50
[Image in the official label — see DailyMed source]
DailyMed Set ID: b6c5522f-209d-6865-e053-2995a90ac8d8 · Version 2
NDC: 81240-001