NDC 51672-1354 - 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
51672-1354
Package NDCs from labels
51672-1354-5, 51672-1354-1, 51672-1354-0, 51672-1354-2
Manufacturer
Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd | Teva Pharmaceutical Works Private Limited Company | Taro Pharmaceutical Industries Ltd.
Effective date
2023-09-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Mupirocin Ointment USP, 2%Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd | Teva Pharmaceutical Works Private Limited Company | Taro Pharmaceutical Industries Ltd.2023-09-27PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-1354-0Mupirocin22 g in 1 TUBEOINTMENT226
51672-1354-0Mupirocin1 in 1 CARTONOINTMENT16
51672-1354-1Mupirocin15 g in 1 TUBEOINTMENT156
51672-1354-1Mupirocin1 in 1 CARTONOINTMENT16
51672-1354-2Mupirocin1 in 1 CARTONOINTMENT16
51672-1354-2Mupirocin30 g in 1 TUBEOINTMENT306
51672-1354-5Mupirocin5 g in 1 TUBEOINTMENT56
51672-1354-5Mupirocin1 in 1 CARTONOINTMENT16

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-1354MUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]58 package rows20230928_86248181-cdd7-4eaf-8b1a-ef5c1b301d06.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
MupirocinACTIVE INGREDIENTD0GX863OA5MUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]1
MupirocinACTIVE MOIETYD0GX863OA5MUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]1
polyethylene glycol 3350INACTIVE INGREDIENTG2M7P15E5PMUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]1
polyethylene glycol 400INACTIVE INGREDIENTB697894SGQMUPIROCIN OINTMENT [TARO PHARMACEUTICALS U.S.A., INC.]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 4 of 13 · 259 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
foster and thrive clearlaxPOLYETHYLENE GLYCOL 3350Strategic Sourcing Services LLC684e35cc-5a4f-458d-b5e7-e1933fea11392026-03-07WarningsExact identifier
unii: G2M7P15E5P
Artificial TearsGLYCERINPreferred Pharmaceuticals Inc.dd646c72-8f47-43c6-a734-db0dcc8cd4d12026-03-06WarningsExact identifier
unii: B697894SGQ
ez2go Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350Valley Medical Products, LLCd64517d6-b0cc-4ba2-b260-e52faa8d4e782026-02-20WarningsExact identifier
unii: G2M7P15E5P
Topcare ClearLaxPOLYETHYLENE GLYCOL 3350Topco Associates LLC03291fd3-7b64-4b79-ad84-e1b9b30a6b032026-02-19WarningsExact identifier
unii: G2M7P15E5P
Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350American Health Packaging81374641-e54c-4b41-a3ad-49b19a0976662026-02-18WarningsExact identifier
unii: G2M7P15E5P
GoodSense Eye Drops Advanced Relief MoisturizerDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLSportpharm LLC8d58dcbb-72a0-41f0-9eeb-613072a6d7ae2026-02-06WarningsExact identifier
unii: B697894SGQ
MUPIROCINMUPIROCINRedpharm Drug49eb7289-c44d-75e1-e063-6294a90a22832026-02-03Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
mupirocinMUPIROCINREMEDYREPACK INC.290b4e51-59b4-429a-987b-715ac817ef2c2026-01-28Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350GLENMARK THERAPEUTICS INC., USA5aba6bb1-d25d-4901-8e9c-4cd4a3a064712026-01-27WarningsExact identifier
unii: G2M7P15E5P
Good Sense Clear LaxPOLYETHYLENE GLYCOL 3350Preferred Pharmaceuticals Inc.935f05da-3637-4a9e-843e-1f2ced5d1a742026-01-23WarningsExact identifier
unii: G2M7P15E5P
MupirocinMUPIROCINAvPAK8b10c706-ae9c-fc76-e053-2a95a90a4c732026-01-20Warnings, Adverse reactionsExact identifier
rxcui: 106346
unii: D0GX863OA5
Polyethylene Glycol 3350POLYETHYLENE GLYCOL 3350YYBA Corp48488531-5d04-4af6-e063-6294a90afe4b2026-01-13WarningsExact identifier
unii: G2M7P15E5P
Lubricant Eye Drops SolutionPOLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOLAvPAKf5743b38-e3d2-a065-e053-2995a90a4b9a2026-01-08WarningsExact identifier
unii: B697894SGQ
Value Health by Prodose Eye DropsTETRAHYDROZOLINE HYDROCHLORIDE AND POLYETHYLENE GLYCOL 400Prodose, Inc.3fafa362-a8a6-3f91-e063-6394a90a98b32025-12-31WarningsExact identifier
unii: B697894SGQ
Signature Care Eye Drops High PerformancePOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLBetter Living Brands LLC6f1f4f58-3208-4b06-9afb-c4beeed093142025-12-30WarningsExact identifier
unii: B697894SGQ
Target Lubricant Eye Drops High PerformancePOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLTarget Corporation6c449374-8847-4c4a-9073-1951ff31d4042025-12-30WarningsExact identifier
unii: B697894SGQ
Target Lubricant Eye Drops High PerformancePOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLTarget Corporationddc15dac-fbd8-42fa-80db-79f49fc6b9eb2025-12-30WarningsExact identifier
unii: B697894SGQ
CVS Advanced Eye DropsDEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HYDROCHLORIDECVS Pharmacy, Inc.f74a2fca-902c-f68a-e053-6394a90abb882025-12-30WarningsExact identifier
unii: B697894SGQ
CVS Hydration Eye DropsPOLYETYLENE GLYCOL 400, PROPYLENE GLYCOLCVSecab8fa3-6575-0dde-e053-2a95a90abd612025-12-30WarningsExact identifier
unii: B697894SGQ
GoodSense Eye Drops Advanced Relief MoisturizerDEXTRAN, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCLGeiss, Derstin & Dunn, Inc.9b34de99-13df-201a-e053-2a95a90ae5592025-12-30WarningsExact identifier
unii: B697894SGQ

Reported adverse events (FAERS/openFDA)#

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