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Bacitracin - Medication Information

Product NDC Code 59898-720
Drug Name

Bacitracin

Type Generic
Pharm Class Decreased Cell Wall Synthesis & Repair [PE]
Active Ingredients
Bacitracin zinc 500 [iu]/g
Route TOPICAL
Dosage Form OINTMENT
RxCUI drug identifier 1366116
Application Number part333B
Labeler Name Water-Jel Technologies
Packages
Package NDC Code Description
59898-720-01 1728 packet in 1 carton (59898-720-01) / .9 g in 1 packet
59898-720-02 144 packet in 1 box, unit-dose (59898-720-02) / .9 g in 1 packet
59898-720-03 25 packet in 1 box, unit-dose (59898-720-03) / .9 g in 1 packet
59898-720-36 .9 g in 1 packet (59898-720-36)
Check if available Online

Active ingredient

A list of the active, medicinal ingredients in the drug product.
Active ingredient Bacitracin zinc 500 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 the affected area apply a small amount of the product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily may be covered with a sterile bandage

Inactive ingredient

A list of inactive, non-medicinal ingredients in a drug product.
Inactive ingredient petrolatum

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 burns

Purpose

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

Spl product data elements

Usually a list of ingredients in a drug product.
Bacitracin Bacitracin BACITRACIN ZINC BACITRACIN PETROLATUM

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 BAUD

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.
Other information store at room temperature do not use any opened or torn packets you may report a serious adverse reaction to this product to 800-275-3433

Ask doctor

Information about when a doctor should be consulted about existing conditions or sumptoms before using the drug product, including all warnings for persons with certain preexisting conditions (excluding pregnancy) and all warnings for persons experiencing certain symptoms. The warnings under this heading are those intended only for situations in which consumers should not use the product until a doctor is consulted.
Ask a doctor before use if you have a deep or puncture wounds, animal bites or serious burns

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 in the eyes or over large areas of the body if you are allergic to any of the ingredients longer than 1 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 the 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? 1-800-276-3433 [email protected] www.waterjel.com Manufactured by Water-Jel Technologies, Inc 50 Broad St., Carlstadt NJ 07072 USA

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 the condition persists or gets worse a rash or other allergic reaction develops

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 Do not use in the eyes or over large areas of the body if you are allergic to any of the ingredients longer than 1 week unless directed by a doctor Ask a doctor before use if you have a deep or puncture wounds, animal bites or serious burns Stop use and ask a doctor if the condition persists or gets worse a rash or other allergic reaction develops Keep out of the reach of children If swallowed, get medical help or contact a Poison Control Center right away.

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

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