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Goodearth sanitizing wipes - Medication Information

Product NDC Code 71745-003
Drug Name

Goodearth sanitizing wipes

Type Brand
Active Ingredients
Benzalkonium chloride 3.822 mg/1
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 1038558
Application Number 505G(a)(3)
Labeler Name GoodEarth Distribution LLC
Packages
Package NDC Code Description
71745-003-01 2 bag in 1 case (71745-003-01) / 1500 cloth in 1 bag
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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 · Wet hands thoroughly with product and allow to dry. · Be sure to use entire wipe. · Discard after single use. · Children under 6 years of age should be supervised when using this product.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients Benzoic Acid, Caprylyl/Capryl Oligoglucoside, Dehydroacetic Acid, Phenoxyethanol, Poly(Laurylglucoside)-7, Propylene Glycol, 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.
Use Hand sanitizer to help reduce bacteria on the skin. Recommended for repeated use.

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
GoodEarth Sanitizing Wipes Benzalkonium Chloride PROPYLENE GLYCOL BENZALKONIUM CHLORIDE BENZALKONIUM DEHYDROACETIC ACID POLY(LAURYLGLUCOSIDE)-7 BENZOIC ACID WATER PHENOXYETHANOL CAPRYLYL/CAPRYL OLIGOGLUCOSIDE

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.
3000 Total Wipes (1500 wipes per roll; 2 rolls per case) NDC: 71745-003-01 Product Label - 1500 SHEETS

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.

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.
Discontinue use if irritation and redness develop. If conditions persist for more than 72 hours, consult a physician. If swallowed get medical help or contact a poison control center immediately.

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 do not use in or near the eyes. In case of contact, rinse eyes thoroughly in 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.

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