Active Ingredient
Bacitracin zinc 500 units
Neomycin sulfate equivalent to 3.5 mg of neomycin base
Polymyxin B 10,000 units as polymyxin B
Sojo Triple Antibiotic Ointment
FDA Label NDC 85248-169
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Jiangxi Yudexi Pharmaceutical Co., Ltd for the product Sojo Triple Antibiotic (NDC 85248-169). 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 ingredient, purpose, use, warnings, do not use, when using, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
First aid antibiotic
Use
first aid to help prevent infection in minor: .cuts .scrapes .burns
Warnings
For external use only.
Do Not Use
.if you are allergic to any of the ingredients .in the eyes .over large areas of the body
When Using
.deep or puncture wounds .animal bites .serious burns
Stop Use
.you need to use longer than l week .condition persists or gets worse .rash or other allergic reaction develops
Ask Doctor
.deep or puncture wounds .animal bites .serious burns
Keep Oot Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.(1-800-222-1222)
Directions
.clean the affected area .apply a small amount of this product (an amount equalto the surface area of the tip of a finger)on the area l to 3 times daily .may be covered with a sterile bandage
Other Information
.store at 20-25°C(68-77°F)
Inactive Ingredients
cocoa butter, cottonseed oil, olive oil, sodium pyruvate, tocopheryl acetate.white petrolatum
Principal Display Panel
3.5 (1cd736a8906806af6c7e5a46523ac894)
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