FDA.reportPublic FDA data

NDC 51672-1312-01 - Mupirocin

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
51672-1312
Requested NDC
51672-1312-01
Package NDCs from labels
51672-1312-1, 51672-1312-0, 51672-1312-2, 51672-1312-01
Manufacturer
Sportpharm LLC
Effective date
2026-05-12
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mupirocin - Sportpharm LLCSportpharm LLC2026-05-12HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - PAI Holdings, LLC dba PAI PharmaPAI Holdings, LLC dba PAI Pharma2026-03-17HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - AvPAKAvPAK2026-01-20HUMAN PRESCRIPTION DRUG LABEL
MupirocinSun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Taro Pharmaceutical Industries Ltd.2025-07-07HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Lohxa | Lohxa LLCLohxa | Lohxa LLC2025-03-25HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Advanced Rx Pharmacy of Tennessee, LLCAdvanced Rx Pharmacy of Tennessee, LLC2024-12-31HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - MAJOR PHARMACEUTICALSMAJOR PHARMACEUTICALS2024-12-31HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Preferred Pharmaceuticals Inc.Preferred Pharmaceuticals Inc.2024-07-22HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Redpharm DrugRedpharm Drug2024-06-29HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2024-06-06HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - REMEDYREPACK INC.REMEDYREPACK INC.2024-02-28HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - RPK Pharmaceuticals, Inc.RPK Pharmaceuticals, Inc.2023-06-07HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Proficient Rx LPProficient Rx LP2023-01-01HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Preferred Pharmaceuticals, Inc.Preferred Pharmaceuticals, Inc.2019-11-01HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - Lake Erie Medical DBA Quality Care Products LLCLake Erie Medical DBA Quality Care Products LLC2019-04-24HUMAN PRESCRIPTION DRUG LABEL
Mupirocin - LohxaLohxa2018-04-03HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-1312-0Mupirocin22 g in 1 TUBEOINTMENT2211
51672-1312-0Mupirocin1 in 1 CARTONOINTMENT111
51672-1312-1Mupirocin15 g in 1 TUBEOINTMENT1511
51672-1312-1Mupirocin1 in 1 CARTONOINTMENT111
51672-1312-2Mupirocin1 in 1 CARTONOINTMENT111
51672-1312-2Mupirocin30 g in 1 TUBEOINTMENT3011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-1312MUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]10Current NDC, Legacy NDC, 6 package rows20230203_900bb675-2f03-47e3-854e-257ec4831332.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-1312-0GM - Gram51672-1312d6b135a5-57bb-4491-88b2-415997e9f34512012-07-24
51672-1312-1GM - Gram51672-131266ed742f-057e-4a20-83ea-82bde7ad7e7312017-05-03

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MupirocinACTIVE INGREDIENTD0GX863OA5MUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]4
MupirocinACTIVE MOIETYD0GX863OA5MUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]4
polyethylene glycol 3350INACTIVE INGREDIENTG2M7P15E5PMUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]4
polyethylene glycol 400INACTIVE INGREDIENTB697894SGQMUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]4
MupirocinACTIVE INGREDIENTD0GX863OA5MUPIROCIN OINTMENT [PREFERRED PHARMACEUTICALS, INC.]2
MupirocinACTIVE MOIETYD0GX863OA5MUPIROCIN OINTMENT [PREFERRED PHARMACEUTICALS, INC.]2
polyethylene glycol 3350INACTIVE INGREDIENTG2M7P15E5PMUPIROCIN OINTMENT [PREFERRED PHARMACEUTICALS, INC.]2
polyethylene glycol 400INACTIVE INGREDIENTB697894SGQMUPIROCIN OINTMENT [PREFERRED PHARMACEUTICALS, INC.]2
MupirocinACTIVE INGREDIENTD0GX863OA5MUPIROCIN OINTMENT [PROFICIENT RX LP]1
MupirocinACTIVE MOIETYD0GX863OA5MUPIROCIN OINTMENT [PROFICIENT RX LP]1
polyethylene glycol 3350INACTIVE INGREDIENTG2M7P15E5PMUPIROCIN OINTMENT [PROFICIENT RX LP]1
polyethylene glycol 400INACTIVE INGREDIENTB697894SGQMUPIROCIN OINTMENT [PROFICIENT RX LP]1

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 3 of 14 · 267 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
GAVILAXPOLYETHYLENE GLYCOL 3350Preferred Pharmaceuticals, Inc.21654def-5ae0-422d-961b-1fe2456af00a2026-05-04WarningsExact identifier
unii: G2M7P15E5P
GoodSense Eye Drops Advanced Relief MoisturizerDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLPreferred PHarmaceuticals Inc.011473a8-26d5-4661-b3c0-745f9b6aa1d82026-04-29WarningsExact identifier
unii: B697894SGQ
POLYETHYLENE GLYCOL 3350POLYETHYLENE GLYCOL 3350CARDINAL HEALTH 110, LLC. DBA LEADER04cc4f2e-1725-4710-8cfb-73a6bdf52e4f2026-04-23WarningsExact identifier
unii: G2M7P15E5P
Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350Aurobindo Pharma Limitedb51f2223-8266-4d6c-bf32-58e53e73b54d2026-04-23WarningsExact identifier
unii: G2M7P15E5P
COMFORTLAXPOLYETHYLENE GLYCOL 3350Family Dollar Stores, LLC02a44a41-0039-f6ec-e063-6394a90ae6f12026-04-23WarningsExact identifier
unii: G2M7P15E5P
Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350Aurohealth LLCd3c77f3f-57aa-4e2d-88aa-731cbb22af702026-04-23WarningsExact identifier
unii: G2M7P15E5P
PEG 3350 and ElectrolytesPOLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDEWilshire Pharmaceuticals, Inc.b251752d-7750-482a-9364-0acf4ad47cc82026-04-16Warnings, Adverse reactionsExact identifier
unii: G2M7P15E5P
GoLYTELYPOLYETHYLENE GLYCOL 3350, SODIUM SULFATE ANHYDROUS, SODIUM BICARBONATE, SODIUM CHLORIDE, POTASSIUM CHLORIDEAzurity Pharmaceuticals, Inc.7609ecf7-0ce0-4fbb-9c27-30987f6895752026-04-15Warnings, Adverse reactionsExact identifier
unii: G2M7P15E5P
TRILYTEPOLYETHYLENE GLYOCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE AND POTASSIUM CHLORIDEAurobindo Pharma Limited79f5e596-8d51-4227-afcc-f5e3411509572026-04-15Warnings, Adverse reactionsExact identifier
unii: G2M7P15E5P
PEG 3350, sodium chloride, sodium bicarbonate and potassium chloridePOLYETHYLENE GLYCOL 3350, SODIUM CHLORIDE, SODIUM BICARBONATE, POTASSIUM CHLORIDEWilshire Pharmaceuticals, Inc.4e442a72-b13b-4869-8a1d-59356095b0912026-04-14Warnings, Adverse reactionsExact identifier
unii: G2M7P15E5P
Retaine Ultra PFPOLYETHYLENE GLYCOLOCuSOFT LLCa5aaaf06-772d-44d3-8601-f978ddc48ad72026-04-13WarningsExact identifier
unii: B697894SGQ
clear laxPOLYETHYLENE GLYCOL 3350Meijer Distribution Inc6464f12c-0883-46c5-943b-a84fe235588e2026-04-13WarningsExact identifier
unii: G2M7P15E5P
equate clear laxPOLYETHYLENE GLYCOL 3350Wal-Mart Stores Inc56a507f3-0cd1-4f02-9dfd-de297ba4bc1f2026-03-27WarningsExact identifier
unii: G2M7P15E5P
Crocodile Tears Lubricant Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400Crocodile Tears LLC4df29336-ea0c-0484-e063-6294a90a685a2026-03-26WarningsExact identifier
unii: B697894SGQ
Artificial Tears Lubricant Eye DropsGLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400KC Pharmaceuticals, Inc4de5c844-85ca-ff9f-e063-6394a90ac12c2026-03-25WarningsExact identifier
unii: B697894SGQ
MUPIROCINMUPIROCINDIRECT RXf88eea1a-2ba1-48bf-96c8-d96d18752aaa2026-03-20Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
BLINK TRIPLE CAREPOLYETHYLENE GLYCOL 400Bausch & Lomb Incorporateda2b34eb0-001b-4f42-a8cc-c2a0150fafcc2026-03-20WarningsExact identifier
unii: B697894SGQ
MupirocinMUPIROCINPAI Holdings, LLC dba PAI Pharmaa822d44d-c651-406c-a2b9-aa8fbe8f89ce2026-03-17Warnings, Adverse reactionsExact identifier
application number: ANDA065170
ndc (package): 0121-1076-01
ndc (package): 0121-1076-50
ndc (product): 0121-1076
rxcui: 106346
spl id: 8427d472-619e-41ef-ae3c-a534b8a9255b
spl set id: a822d44d-c651-406c-a2b9-aa8fbe8f89ce
unii: D0GX863OA5
Leader Ultra Lubricating Eye DropsPOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLCardinal Healthd7f011a2-05ba-47c3-9519-d31602e105c72026-03-12WarningsExact identifier
unii: B697894SGQ
Leader Advanced Relief Eye DropsDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLCardinal Health5c5d6c13-9b51-48f0-8627-b60b0f707fd32026-03-12WarningsExact identifier
unii: B697894SGQ

Reported adverse events (FAERS/openFDA)#

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