Sign In

Save up to 80% by drug discount in your pharmacy with "Pharmacy Near Me - National Drug Discount Card"

You can scan QR Code(just open camera on your phone/scan by application) from the image on prescription drug discount card to save it to your mobile phone. Or just click on image if you're on mobile phone.

View Generic:
View Brand:

Swisher - Medication Information

Product NDC Code 47593-576
Drug Name

Swisher

Type Brand
Active Ingredients
Benzalkonium chloride 1 mg/ml
Route TOPICAL
Dosage Form SOLUTION
RxCUI drug identifier 1038799
Application Number part333E
Labeler Name Ecolab Inc.
Packages
Package NDC Code Description
47593-576-30 207 ml in 1 bottle, plastic (47593-576-30)
47593-576-41 750 ml in 1 bottle, plastic (47593-576-41)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Benzalkonium chloride 0.1%

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 wash hands to remove soil dispense palmful spread to cover hands, rub in well air dry, do not rinse or towel dry

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients water (aqua), isopropyl alcohol, propylene glycol, FD&C red 40, FD&C blue 1

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 for handwashing to decrease bacteria on the skin

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Swisher Benzalkonium chloride BENZALKONIUM CHLORIDE BENZALKONIUM WATER ISOPROPYL ALCOHOL PROPYLENE GLYCOL FD&C RED NO. 40 FD&C BLUE NO. 1

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.
Representative label and principal display panel SWISHER Foodservice Foaming Hand Sanitizer Active Ingredient: Benzalkonium chloride 0.1% 6101426 750 mL (25 US FL OZ) Active ingredient | Benzalkonium chloride 0.1% 767264/5402/0619 This product may be patented www.ecolab.com/patents For questions or comments, call 1-866-444-7450. Ecolab · 1 Ecolab Place · St Paul MN 55102 USA © 2019 Ecolab USA Inc. · All rights reserved Made in U.S.A. representative label

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 in eyes

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.

Questions

A telephone number of a source to answer questions about a drug product. Sometimes available days and times are also noted.
Questions? call 1.800.35.CLEAN (352.5326)

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 doctor if skin irritation or redness persists 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.
When using this product if in eyes, rinse promptly and throughly with water discontinue use if irritation and redness develop

References

This field may contain references when prescription drug labeling must summarize or otherwise relay on a recommendation by an authoritative scientific body, or on a standardized methodology, scale, or technique, because the information is important to prescribing decisions.
Other information for additional information, see Safety Data Sheet (SDS) for emergency medical information in USA and Canada, call 1.800.328.0026 for emergency medical information worldwide, call 1.651.222.5352 (in USA)

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 FLAMMABLE. Keep away from fire or flame, heat, sparks, and sources of static discharge. Do not use in eyes When using this product if in eyes, rinse promptly and throughly with water discontinue use if irritation and redness develop Stop use and ask doctor if skin irritation or redness persists for more than 72 hours 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