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Nimbus

Dosage form
CLOTH
Labeler
Nimbus Eco Inc.
Label updated
2022-01-13
Retrieved
2026-09-07
Active ingredients
BENZALKONIUM CHLORIDE
View original label and images on DailyMed ↗
Label information

This is a hand sanitizing wipe manufactured using only the following United States Pharmacopoeia (USP) grade ingredients

  1. Benzalkonium Chloride (USP grade) (0.12%, volume/volume (v/v))
  2. 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