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First aid antispetic - Medication Information

Product NDC Code 49314-0001
Drug Name

First aid antispetic

Type Brand
Active Ingredients
Benzalkonium chloride .13 mg/ml
Route TOPICAL
Dosage Form SPRAY
Application Number part333A
Labeler Name Unishield
Packages
Package NDC Code Description
49314-0001-1 59.1 ml in 1 bottle, spray (49314-0001-1)
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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 clean affected area & spray 1 to 3 times daily may be covered with a sterile bandage not to be used on children under 12 of years of age

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients ethyl alcohol, 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 first aid to help prevent infection in minor cuts, scrapes and burns

Purpose

Information about the drug product’s indications for use.
Purpose First aid antiseptic

Spl product data elements

Usually a list of ingredients in a drug product.
First Aid Antispetic Benzalkonium Chloride WATER ALCOHOL BENZALKONIUM CHLORIDE BENZALKONIUM

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.
Package Label - Principal Display Panel image of bottle 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 near eyes or mucous membranes on deep or puncture wounds , animal bites, or serious burns over large areas of the body more than one week unless directed by a doctor

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 or comments? 1-800-480-5855

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 a doctor if condition persists or gets worse

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

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