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Germisept antibacterial hand sanitizing wipes - Medication Information

Product NDC Code 70335-301
Drug Name

Germisept antibacterial hand sanitizing wipes

Type Brand
Active Ingredients
Benzalkonium chloride .12 g/100g
Route TOPICAL
Dosage Form LIQUID
RxCUI drug identifier 1038741
Application Number part333E
Labeler Name Innovent Inc.
Packages
Package NDC Code Description
70335-301-08 8 patch in 1 package (70335-301-08) / 30 g in 1 patch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzalkhonium Chloride 0.12% Purpose Antibacterial

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 hands 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 ingredients Aqua (Purified & De-Ionized Water), Aloe Barbadensis Leaf Extract, Citric Acid, Didecyldimonium Chloride, 2-Bromo-2-Nitropropane-1,3-Diol, Polyaminopropyl Biguanide, Parfum (Fragrance).

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.
Uses Decrease bacteria on the skin.

Purpose

Information about the drug product’s indications for use.
Purpose Antibacterial

Spl product data elements

Usually a list of ingredients in a drug product.
GERMISEPT Antibacterial Hand Sanitizing Wipes BENZALKONIUM CHLORIDE ALOE VERA LEAF CHAMOMILE CITRIC ACID MONOHYDRATE IODOPROPYNYL BUTYLCARBAMATE LAURYL GLUCOSIDE PHENOXYETHANOL PROPYLENE GLYCOL EDETATE SODIUM WATER BENZALKONIUM CHLORIDE BENZALKONIUM

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.
Package Labeling: image description

Spl unclassified section

Information not classified as belonging to one of the other fields. Approximately 40% of labeling with effective_time between June 2009 and August 2014 have information in this field.
Other information • Store below 95° F (35° C) to prevent from drying out. • Dispose of wipe in the proper container. • Do not flush down the toilet.

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.

When using

Information about side effects that people may experience, and the substances (e.g. alcohol) or activities (e.g. operating machinery, driving a car) to avoid while using the drug product.
When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water.

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. When using this product avoid contact with eyes. If contact occurs, rinse thoroughly with water. Discontinue use if irritation and redness develop. If condition persists for more than 72 hours consult a doctor. Keep out of reach of children. If swallowed, get medical help or contact Poison Control Center right away.

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