FDA.reportPublic FDA data

Triple Antibiotic and Pain Relief

Product NDC
59779-823
Requested package NDC
59779-823-56
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

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage59779-82359779-823-56DDiscontinued by firm2026-10-05

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 · 9 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-100efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDCEffectiveRelated label
59779-823-342023-10-09Triple Antibiotic & Pain Relief Maximum Strength Ointment - CVS
59779-823-562023-10-09Triple Antibiotic & Pain Relief Maximum Strength Ointment - CVS
59779-823-342023-01-30Triple Antibiotic & Pain Relief Maximum Strength Ointment - CVS
59779-823-562023-01-30Triple Antibiotic & Pain Relief Maximum Strength Ointment - CVS

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59779-823-34GM - Gram59779-82362fa32c7-4a94-41c9-8fa2-a4abfeeb519212019-02-13
59779-823-56GM - Gram59779-82308375784-9afd-4ad1-b231-06679c2e051312018-07-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BACITRACIN ZINCACTIVE INGREDIENT89Y4M234ESTRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
NEOMYCIN SULFATEACTIVE INGREDIENT057Y626693TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
POLYMYXIN B SULFATEACTIVE INGREDIENT19371312D4TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
PRAMOXINE HYDROCHLORIDEACTIVE INGREDIENT88AYB867L5TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
BACITRACINACTIVE MOIETY58H6RWO52ITRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
NEOMYCINACTIVE MOIETYI16QD7X297TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
POLYMYXIN BACTIVE MOIETYJ2VZ07J96KTRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
PRAMOXINEACTIVE MOIETY068X84E056TRIPLE ANTIBIOTIC AND PAIN RELIEF MAXIMUM STRENGTH (BACITRACIN ZINC, NEOMYCIN SULFATE, POLYMYXIN B SULFATE AND PRAMOXINE HYDROCHLORIDE) OINTMENT [CVS PHARMACY]3
PETROLATUMINACTIVE INGREDIENT4T6H12BN9UTRIPLE 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 NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
59779-823-56597790823561 TUBE in 1 CARTON (59779-823-56) > 28 g in 1 TUBE1 tube2005-01-030000-00-00NoNoCurrent