Active Ingredients
- Bacitracin Zinc 400 units
- Neomycin Sulfate 3.5mg
- Polymyxin B Sulfate 5,000 units
Olp Triple Antibiotic
FDA Label NDC 70648-555
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Ohio Lab Pharma for the product Olp Triple Antibiotic (NDC 70648-555). 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 active ingredients, purpose, uses, warnings, otc - ask doctor, stop use and ask a doctor if, otc - do not use, 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
Purpose
First aid antibiotic
Uses
First aid to help prevent infection in minor:
- cuts
- scrapes
- burns
Warnings
- For external use only
Otc - Ask Doctor
Ask a doctor before use if you have
- serious burns
- deep or puncture wounds
- animal bites
Stop Use And Ask A Doctor If
Stop use and ask a doctor if
- condition persists or gets worse
- rash or other allergic reaction develops
Otc - Do Not Use
do not use:
- do not use in the eyes
- do not apply over large areas of the body
- if you are allergic to any of the ingredients
- longer than one week unless directed by your doctor
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 tot the surface area of the tip of a finer) on the area 1 to 3 times daily
- may be covered with a sterile bandage
Other Information
- store at room temperature
Inactive Ingredient
Petrolatum
Questions
www.ohiolabpharma.us
Package Label.Principal Display Panel
ORIGINAL OINTMENT
NET WEIGHT: 0.33OZ (9.4g)
NDC#70648-555-01
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