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Ever ready first aid triple antibiotic - Medication Information

Product NDC Code 72976-009
Drug Name

Ever ready first aid triple antibiotic

Type Brand
Pharm Class Aminoglycoside Antibacterial [EPC],
Aminoglycosides [CS],
Decreased Cell Wall Synthesis & Repair [PE],
Polymyxin-class Antibacterial [EPC],
Polymyxins [CS]
Active Ingredients
Bacitracin zinc 400 [usp'u]/g
Neomycin sulfate .0035 g/g
Polymyxin b sulfate 5000 [usp'u]/g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 204602
Application Number M004
Labeler Name EVER READY FIRST AID
Packages
Package NDC Code Description
72976-009-01 .9 g in 1 pouch (72976-009-01)
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Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredients (in each gram) Bacitracin Zinc (400 units Bacitracin) Neomycin sulfate (3.5 mg Neomycin) Polymyxin B sulfate First aid (Polymyxin B 5000 units)

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 apply a small amount 1 to 3 times daily may cover with a sterile bandag

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredients Mineral oil, Petroleum, 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 antibiotic

Spl product data elements

Usually a list of ingredients in a drug product.
Ever Ready First Aid Triple Antibiotic Bacitracin zinc, Neomycin sulfate, Polymyxin B sulfate BACITRACIN ZINC BACITRACIN NEOMYCIN SULFATE NEOMYCIN POLYMYXIN B SULFATE POLYMYXIN B MINERAL OIL PETROLATUM WATER

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.
image of pouch 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 internally in eyes over large areas of the body or on puncture wounds, animal bites or serious burns for more then 1 week unless directed by a doctor if you are allergic to any of the ingredients

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 ingested, contact a Poison Control Center right away.

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 a rash or allergic reaction develops condition worsens or persists

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