Medichoice Bacitracin Ointment
FDA Label NDC 39892-0810
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by O&m Halyard, Inc. for the product Medichoice Bacitracin (NDC 39892-0810). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding drug facts, active ingredient (in each gram), purpose, uses, warnings, do not use:, stop use and ask a doctor:, keep out of reach of children., and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient (In Each Gram)
Bacitracin 500 units
Purpose
First aid antibiotic
Uses
First aid to help prevent infection in:
• minor cuts • scrapes • burns
Warnings
• for external use only
Do Not Use:
• in the eyes
• if you are allergic to any of the ingredients, due to the possibility of anaphylactic shock
• over large areas of the body
• longer than 1 week unless directed by a doctor
Stop Use And Ask A Doctor:
• before use in case of deep puncture wounds, animal bites or serious burns
• if the condition persists or gets worse
• if a rash or other allergic reaction develops
Keep Out Of Reach Of Children.
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
• clean the affected area
• apply a small amount of this 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
Other Information:
• Tamper Evident. Do not use if package is torn, cut or opened.
• Avoid excessive heat and humidity
• Store at a controlled room temperature 15˚ to 30˚C (59˚ to 86˚F)
Inactive Ingredients
white petrolatum.
* Please review the disclaimer below.
