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Multi-purpose antibacterial wet wipes - Medication Information

Product NDC Code 79531-003
Drug Name

Multi-purpose antibacterial wet wipes

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100g
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 1038558
Application Number part333A
Labeler Name Supreme Premium Products,Inc.
Packages
Package NDC Code Description
79531-003-01 77 g in 1 bag (79531-003-01)
79531-003-02 295 g in 1 bag (79531-003-02)
79531-003-03 435 g in 1 pail (79531-003-03)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient(s) Benzalkonium Chloride 0.13%

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 using a label attached, pull out the wipe, and then seal the opening by sticking back the label to prevent the wipe from drying out.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients C12-14 Alkyl Dimethyl, Ethylbenzyl Ammonium Chloride, Alkyl Polyglucoside, Disodium EDTA, Propylene Glycol, Aqua.

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.
Use Decreases bacteria on skin.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Multi-purpose Antibacterial Wet Wipes BENZALKONIUM CHLORIDE N-ALKYL ETHYLBENZYL DIMETHYL AMMONIUM CHLORIDE (C12-C14) DECYL GLUCOSIDE WATER BENZALKONIUM CHLORIDE BENZALKONIUM PROPYLENE GLYCOL EDETATE DISODIUM

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 Label - Principal Display Panel label-15 label-15-2 label-60 label-60-2 label-75

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.
Drug Facts

Do not use

Information about all contraindications for use. These contraindications are absolute and are intended for situations in which consumers should not use the product unless a prior diagnosis has been established by a doctor or for situations in which certain consumers should not use the product under any circumstances regardless of whether a doctor or health professional is consulted.
Do not use Do not use if you are allergic to any of the ingredients.

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 a Poison Control Center right away.

Stop use

Information about when use of the drug product should be discontinued immediately and a doctor consulted. Includes information about any signs of toxicity or other reactions that would necessitate immediately discontinuing use of the product.
Stop use and ask a doctor if irritation or rash develops and continues for more than 72 hours.

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.
Using this product do not get into eyes. lf contact occurs, rinse thoroughly with water.

Storage and handling

Information about safe storage and handling of the drug product.
Other information The expiry date is stated on the packaging, Store at -20℃ to +30℃,away from sunlight.

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.

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