Home NDC 59779-823 Triple Antibiotic and Pain Relief
Product NDC 59779-823
11-digit product format 597790823
Labeler code 59779
Product ID 59779-823_46c24560-2681-4acd-abce-818517c5fb47
Type HUMAN OTC DRUG
Nonproprietary name bacitracin zinc, neomycin sulfate, polymyxin b sulfate and pramoxine hydrochloride
Dosage form OINTMENT
Route TOPICAL
Labeler CVS Pharmacy
Application part333B
Marketing category OTC MONOGRAPH FINAL
Marketing start 2005-01-03
Marketing end 0000-00-00
Substance BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
Active strength 500 [USP'U]/g; mg/g; [USP'U]/g; mg/g
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 27 matching rows.
View current auxiliary records. · View the auxiliary file history.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing# DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BACITRACIN ZINC ACTIVE INGREDIENT 89Y4M234ES TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 NEOMYCIN SULFATE ACTIVE INGREDIENT 057Y626693 TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 POLYMYXIN B SULFATE ACTIVE INGREDIENT 19371312D4 TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 PRAMOXINE HYDROCHLORIDE ACTIVE INGREDIENT 88AYB867L5 TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 BACITRACIN ACTIVE MOIETY 58H6RWO52I TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 NEOMYCIN ACTIVE MOIETY I16QD7X297 TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 POLYMYXIN B ACTIVE MOIETY J2VZ07J96K TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 PRAMOXINE ACTIVE MOIETY 068X84E056 TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3 PETROLATUM INACTIVE INGREDIENT 4T6H12BN9U TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY] 3
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 59779-823-34 59779082334 1 TUBE in 1 CARTON (59779-823-34) > 14 g in 1 TUBE 1 tube 2005-01-03 0000-00-00 No No Current 59779-823-56 59779082356 1 TUBE in 1 CARTON (59779-823-56) > 28 g in 1 TUBE 1 tube 2005-01-03 0000-00-00 No No Current