Drugplain

Multi Action 500 [USP'U]/g

Bacitracinzinc,NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL · OINTMENT · Trifecta Pharmaceutical USA LLC

No Recall History
Plain English

Multi Action is a ointment containing bacitracinzinc,neomycinsulfate,polymyxinbsulfate,pramoxinehcl at 500 [USP'U]/g, taken topical. Manufactured by Trifecta Pharmaceutical USA LLC.

Key Facts

Brand Name
Multi Action
Generic Name
Bacitracinzinc,NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL
NDC Code (Product)
69396-072
Manufacturer
Trifecta Pharmaceutical USA LLC
Strength
500 [USP'U]/g
Dosage Form
OINTMENT
Route
TOPICAL
Marketing Status
Application #
M004
Marketing Start
01/22/2021

Recall History

No Recall History

Frequently Asked Questions

What is Multi Action used for?

Multi Action contains Bacitracinzinc,NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL. It is a ointment taken topical. Consult your doctor for specific uses.

Is Multi Action a controlled substance?

Multi Action is not classified as a controlled substance by the DEA.

What is the generic name for Multi Action?

The generic name for Multi Action is Bacitracinzinc,NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL. There are no other listed brand versions of Bacitracinzinc,NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL.

What is the NDC code for Multi Action 500 [USP'U]/g?

The NDC (National Drug Code) for Multi Action 500 [USP'U]/g is 69396-072, listed by Trifecta Pharmaceutical USA LLC.

Product NDC

69396-072

Package NDC

69396-072-01

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)