Label: TRIPLE ANTIBIOTIC ointment
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Contains inactivated NDC Code(s)
NDC Code(s): 70512-102-30 - Packager: SOLA Pharmaceuticals
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
Drug Label Information
Updated July 5, 2022
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- Official Label (Printer Friendly)
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Active Ingerdients (in each gram)
Bacitracin Zinc USP 400 Units - Neomycin Sulfate USP 5mg (equivalent to 3.5mg of Neomycin) Polymixin B Sulfate USP 5,000 Units
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Purpose
First aid antibiotic
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Uses
First aid to help prevent infection in minor: cuts - scrapes - burns
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Warnings
For external use only
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DO NOT USEDo not use: If you are allergic to any of the ingredients - In the eyes - Over large areas of the body
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ASK DOCTORAsk a doctor before use if you have - Deep or puncture wounds - Animal bites - Serious burns - Stop use and ask a doctor if: You need to use longer than 1 week - Condition persists or gets worse - Rash ...
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KEEP OUT OF REACH OF CHILDRENKeep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away
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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 ...
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Other Information
Store at 20-25°C (68-77°F) Store away from heat
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Inactive ingredients
White Petrolatum
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Questions or comments?
Call 1-866-747-7365
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PRINCIPAL DISPLAY PANELManufactured for : SOLA Pharmaceuticals - Baton Rouge, LA 70810 - Triple Antibiotic - NDC 70512-102-30 - Qty: 28.4g
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INGREDIENTS AND APPEARANCEProduct Information
