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Mykro max multi purpose disinfecting wipe - Medication Information

Product NDC Code 71734-322
Drug Name

Mykro max multi purpose disinfecting wipe

Type Brand
Active Ingredients
Benzalkonium chloride .13 g/100g
Route TOPICAL
Dosage Form SWAB
RxCUI drug identifier 1038558
Application Number part333A
Labeler Name JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Packages
Package NDC Code Description
71734-322-01 100 package in 1 canister (71734-322-01) / 3.5 g in 1 package
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient 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 To clean: use fresh wipe to clan and allow to dry naturally. Repeat for better results. Children should be supervised when using this product.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: Phenoxyethanol, Ethylhexylglycerin, DDAC, Propylene Glycol, Glycerin, Purified 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.
Uses: sanitizing wipe for general cleaning.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Mykro Max Multi Purpose Disinfecting wipe benzalkonium chloride benzalkonium chloride BENZALKONIUM water PHENOXYETHANOL ETHYLHEXYLGLYCERIN PROPYLENE GLYCOL GLYCERIN

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.
Principal Display Panel

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.
For external use only. When using this product do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation persists, seek edical attention.

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.

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 do not use in or near the eyes. In case of contact, rinse eyes thoroughly with water. Stop use and ask a doctor if irritation persists, seek edical attention. Keep out of reach of children. if swallowed get medical help or contact a 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