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Accumed antibacterial hand sanitizing wipes - Medication Information

Product NDC Code 81204-001
Drug Name

Accumed antibacterial hand sanitizing wipes

Type Brand
Active Ingredients
Benzalkonium chloride 1.1 mg/ml
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 1303110
Application Number part333A
Labeler Name ACCUMED BIOTECH LLC
Packages
Package NDC Code Description
81204-001-01 30 pouch in 1 pouch (81204-001-01) / 2.9 ml in 1 pouch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Benzalkonium chloride 0.11%

Dosage and administration

Information about the drug product’s dosage and administration recommendations, including starting dose, dose range, titration regimens, and any other clinically sigificant information that affects dosing recommendations.
Directions ■ Open resealable label, remove one wipe to use ■ Wipe hand thoroughly with product and allow to dry without wiping. ■ Close resealable label after use to retain moisture.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredient 2-Bromo-2-Nitropropane-1,3-Diol, Aloe Barbadensis Leaf Extract, Chamomilla Recutita Flower Extract, Citric Acid, Iodopropynyl Butylcarbamate, Lauryl Glucoside, Phenoxyethanol, Polysorbate 20, Propylene Glycol, Sodium Citrate, Tetrasodium EDTA, Water.

Indications and usage

A statement of each of the drug products indications for use, such as for the treatment, prevention, mitigation, cure, or diagnosis of a disease or condition, or of a manifestation of a recognized disease or condition, or for the relief of symptoms associated with a recognized disease or condition. This field may also describe any relevant limitations of use.
For hand washing to decrease bacteria on the skin.

Purpose

Information about the drug product’s indications for use.
Antibacterial ■ For handwashing to decrease bacteria on the skin.

Spl product data elements

Usually a list of ingredients in a drug product.
AccuMed Antibacterial Hand Sanitizing Wipes Benzalkonium Chloride IODOPROPYNYL BUTYLCARBAMATE MATRICARIA CHAMOMILLA FLOWERING TOP OIL DITETRACYCLINE TETRASODIUM EDETATE LAURYL GLUCOSIDE POLYSORBATE 20 SODIUM CITRATE CITRIC ACID MONOHYDRATE ALOE VERA LEAF PHENOXYETHANOL 3-HEXYLOXYPROPYLENE GLYCOL BRONOPOL BENZALKONIUM CHLORIDE BENZALKONIUM WATER

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
A

Keep out of reach of children

Information pertaining to whether the product should be kept out of the reach of children, and instructions about what to do in the case of accidental contact or ingestion, if appropriate.
Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

Warnings

Information about serious adverse reactions and potential safety hazards, including limitations in use imposed by those hazards and steps that should be taken if they occur.
Warnings For external use only. ■ Do not use on eyes. If eye contact occurs, rinse eyes thoroughly with water. ■ Do not flush.■ Discontinue use if irritation and redness develop. If condition persists for more than 72 hours, consult a doctor.

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API