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Hand wipes - Medication Information

Product NDC Code 71734-203
Drug Name

Hand wipes

Type Brand
Pharm Class Decreased Cell Wall Integrity [PE]
Active Ingredients
Benzethonium chloride .08 g/g
Chlorhexidine gluconate .1 g/g
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 1667684
Application Number part333A
Labeler Name JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD.
Packages
Package NDC Code Description
71734-203-01 13.3 g in 1 package (71734-203-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzethonium Chloride .......... 0.08 Chlorhexidine Digluconate ........ 0.10

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 Self-dries in seconds. Leaves skin soft and smooth.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive Ingredients: 5-chloro-2-methyl-2H-isothiazol-3-one, Methylisothiazolinone, Polyaminopropyl Biguanide, Glycerol, 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: Cleans and refreshes hands and face without soap and water

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Hand Wipes Chlorhexidine Digluconate and BENZETHONIUM CHLORIDE CHLORHEXIDINE GLUCONATE CHLORHEXIDINE BENZETHONIUM CHLORIDE BENZETHONIUM GLYCERIN POLYAMINOPROPYL BIGUANIDE Water Methylisothiazolinone

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 on hands only. Stop use and sonsult a doctor if skin irritation develops. Store in a cool place.

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. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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.
For external use only. for external use on hands only. Stop use and sonsult a doctor if skin irritation develops. Store in a cool place. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately.

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