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Antibacterial wipes - Medication Information

Product NDC Code 75109-504
Drug Name

Antibacterial wipes

Type Brand
Active Ingredients
Benzalkonium chloride .3 g/100g
Route TOPICAL
Dosage Form CLOTH
RxCUI drug identifier 1812737
Application Number part333A
Labeler Name Kangna (Zhejiang) Medical Supplies Co., Ltd.
Packages
Package NDC Code Description
75109-504-01 50 pouch in 1 bag (75109-504-01) / 5.5 g in 1 pouch
75109-504-02 10 pouch in 1 package (75109-504-02) / 58 g in 1 pouch
75109-504-03 25 pouch in 1 package (75109-504-03) / 135 g in 1 pouch
75109-504-04 50 pouch in 1 package (75109-504-04) / 270 g in 1 pouch
75109-504-05 80 pouch in 1 package (75109-504-05) / 430 g in 1 pouch
75109-504-06 100 pouch in 1 package (75109-504-06) / 530 g in 1 pouch
75109-504-07 70 pouch in 1 canister (75109-504-07) / 387.845 g in 1 pouch
75109-504-08 100 pouch in 1 canister (75109-504-08) / 316.5 g in 1 pouch
75109-504-09 300 pouch in 1 canister (75109-504-09) / 849.5 g in 1 pouch
75109-504-10 800 pouch in 1 bag (75109-504-10) / 1543.43 g in 1 pouch
75109-504-11 1200 pouch in 1 bag (75109-504-11) / 2300.15 g in 1 pouch
75109-504-12 1500 pouch in 1 bag (75109-504-12) / 2867.69 g in 1 pouch
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active Ingredient Benzalkonium Chloride 0.3% Purpose Antiseptic

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 ●Gently pull back resealable label, remove and use wipe as required. , Reseal back after use.

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Water, Phenoxyethanol, DMDM Hydantoin, Ethylparaben, Methylparaben, Polysorbate 20, Fragrance, Disodium EDTA, Sodium Citrate, Cetylpyridinium Chloride.

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 ●For hand sanitizing to decrease bacteria on the skin. ●Apply topically to the skin to help prevent cross contamination. ●Recommended for repeated use. ●Dries in seconds.

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.
Antibacterial wipes Benzalkonium Chloride CETYLPYRIDINIUM CHLORIDE WATER DMDM HYDANTOIN POLYSORBATE 20 PHENOXYETHANOL ETHYLPARABEN BENZALKONIUM CHLORIDE BENZALKONIUM EDETATE DISODIUM ANHYDROUS METHYLPARABEN SODIUM CITRATE

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.
1

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 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.
Warning ●For external use only. ●Do not use in or contact the eyes. " Stop use and ask a doctor if too much skin irritation or sensitivity develops or increases. ●Keep out of reach of children. If swallowed, get medical help 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