FDA.reportPublic FDA data

NDC 51672-1310-01 - Betamethasone Dipropionate

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
51672-1310
Requested NDC
51672-1310-01
Package NDCs from labels
51672-1310-1, 51672-1310-2, 51672-1310-3, 51672-1310-01
Manufacturer
Preferred Pharmaceuticals, Inc.
Effective date
2026-03-19
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Betamethasone Dipropionate - Preferred Pharmaceuticals, Inc.Preferred Pharmaceuticals, Inc.2026-03-19HUMAN PRESCRIPTION DRUG LABEL
Betamethasone Dipropionate - A-S Medication SolutionsA-S Medication Solutions2026-02-06HUMAN PRESCRIPTION DRUG LABEL
CETEARETH-30 - Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.2025-09-26HUMAN PRESCRIPTION DRUG LABEL
Betamethasone Dipropionate - NuCare Pharmaceuticals,Inc.NuCare Pharmaceuticals,Inc.2025-04-03HUMAN PRESCRIPTION DRUG LABEL
Betamethasone Dipropionate - Asclemed USA, Inc | ASCLEMED USA INC. DBA ENOVACHEMAsclemed USA, Inc | ASCLEMED USA INC. DBA ENOVACHEM2024-10-11HUMAN PRESCRIPTION DRUG LABEL
Betamethasone Dipropionate - REMEDYREPACK INC.REMEDYREPACK INC.2024-03-27HUMAN PRESCRIPTION DRUG LABEL
Betamethasone Dipropionate - RPK Pharmaceuticals, Inc.RPK Pharmaceuticals, Inc.2023-09-11HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-1310-1Betamethasone Dipropionate1 in 1 CARTONCREAM, AUGMENTED18
51672-1310-1Betamethasone Dipropionate15 g in 1 TUBECREAM, AUGMENTED158
51672-1310-2Betamethasone Dipropionate30 g in 1 TUBECREAM, AUGMENTED308
51672-1310-2Betamethasone Dipropionate1 in 1 CARTONCREAM, AUGMENTED18
51672-1310-3Betamethasone Dipropionate1 in 1 CARTONCREAM, AUGMENTED18
51672-1310-3Betamethasone Dipropionate50 g in 1 TUBECREAM, AUGMENTED508

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-1310BETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]5Current NDC, Legacy NDC, 6 package rows20210415_000ae256-a337-4903-845b-003777a4efa8.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-1310-1GM - Gram51672-13101a93637d-5b1c-4b88-9f5f-b66de807912812012-07-24
51672-1310-3GM - Gram51672-13105ea95523-9dc9-4f02-b6db-3e4cf8febea312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
Betamethasone DipropionateACTIVE INGREDIENT826Y60901UBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
BetamethasoneACTIVE MOIETY9842X06Q6MBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
carbomer homopolymer type c (allyl pentaerythritol crosslinked)INACTIVE INGREDIENT4Q93RCW27EBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
ceteareth-30INACTIVE INGREDIENT1R9DCZ5FOXBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
chlorocresolINACTIVE INGREDIENT36W53O7109BETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
cyclomethiconeINACTIVE INGREDIENTNMQ347994ZBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
glyceryl oleateINACTIVE INGREDIENT4PC054V79PBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
petrolatumINACTIVE INGREDIENT4T6H12BN9UBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
propylene glycolINACTIVE INGREDIENT6DC9Q167V3BETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
sodium hydroxideINACTIVE INGREDIENT55X04QC32IBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
sorbitolINACTIVE INGREDIENT506T60A25RBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
waterINACTIVE INGREDIENT059QF0KO0RBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2
white waxINACTIVE INGREDIENT7G1J5DA97FBETAMETHASONE DIPROPIONATE CREAM, AUGMENTED [TARO PHARMACEUTICALS U.S.A., INC.]2

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 7 of 43 · 859 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
SernivoBETAMETHASONE DIPROPIONATEPrimus Pharmaceuticals, Inc.b1b3d1b0-da9b-11eb-ad76-0800200c9a662026-04-22Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
PURE PETROLATUMPETROLATUMMY IMPORTS USA LLC4fba8bc7-590d-f621-e063-6294a90ad8c92026-04-18WarningsExact identifier
unii: 4T6H12BN9U
Equaline HemorrhoidalMINERAL OIL, PETROLATUM, PHENYLEPHRINE HCLUnited Natural Foods, Inc. dba UNFIa6ed1987-37ad-4bfd-8cea-f03426953f5a2026-04-16WarningsExact identifier
unii: 4T6H12BN9U
Artificial Tears Lubricant Eye DropsGLYCERIN, PROPYLENE GLYCOLCVS Pharmacy28297fee-8185-4869-8f39-5bfbf8bf8bfd2026-04-13WarningsExact identifier
unii: 6DC9Q167V3
Retaine Ultra PFPOLYETHYLENE GLYCOLOCuSOFT LLCa5aaaf06-772d-44d3-8601-f978ddc48ad72026-04-13WarningsExact identifier
unii: 6DC9Q167V3
Petroleum JellyWHITE PETROLATUMWAL-MART STORES INC00faa772-53f3-9276-e063-6394a90a2dab2026-04-07WarningsExact identifier
unii: 4T6H12BN9U
PetroleumWHITE PETROLATUMCVS Pharmacy, Inc.4dc08832-e610-4e62-a6af-cadaa339e39e2026-04-06Warnings, Adverse reactionsExact identifier
unii: 4T6H12BN9U
PetroleumWHITE PETROLATUMAmazon.com Services LLC616ef87d-1518-46aa-8e12-9a1b678d49802026-04-06Warnings, Adverse reactionsExact identifier
unii: 4T6H12BN9U
Jack BlackAVOBENZONE/HOMOSALATE/OCTISALATE/PETROLATUMJack Black L.L.C.4baade5c-e759-d98f-e063-6394a90aa0562026-04-03WarningsExact identifier
unii: 4T6H12BN9U
KIDS TOOTHPASTE, FOR CAVITY PROTECTIONKIDS TOOTHPASTE FOR CAVITY PROTECTIONShulisa (Foshan) Daily ChemicalIndustry Co., Ltd4e8fab9e-f05c-5e2f-e063-6294a90aecf92026-04-03WarningsExact identifier
unii: 059QF0KO0R
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATESportpharm LLC313dde2e-fb82-4786-988b-565d3e003c372026-04-01Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
Clotrimazole and Betamethasone DipropionateCLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATEPreferred Pharmaceuticals Inc.196e24fc-3315-4366-ad40-51b7ea54b2112026-04-01Warnings, Adverse reactionsExact identifier
unii: 826Y60901U
Critic-Aid ClearPETROLATUMColoplast Corpa92c18f7-52b2-43e4-bae3-2bab9de226712026-03-31WarningsExact identifier
unii: 4T6H12BN9U
Critic Aid ClearPETROLATUMColoplast Corp0b6da97e-519b-4579-9895-f4ede5c48b472026-03-27WarningsExact identifier
unii: 4T6H12BN9U
Baza ClearPETROLATUMColoplast Corp69d9f456-1a35-4146-8366-c0285648a1722026-03-27WarningsExact identifier
unii: 4T6H12BN9U
Vitamin A DLANOLIN, PETROLATUMTopco Associates LLC5126fdf6-5df5-474b-bc0d-3a82dea61abb2026-03-26Warnings, Adverse reactionsExact identifier
unii: 4T6H12BN9U
Advanced HealingPETROLATUMAmazon.com Services LLCcdf1bd12-ac59-4f06-be0f-ef6eb3caeeff2026-03-26Warnings, Adverse reactionsExact identifier
unii: 4T6H12BN9U
D-CerinMOISTURIZERDynarex Corporation7ea47a7e-12af-9290-e053-2a91aa0a065f2026-03-24WarningsExact identifier
unii: 4T6H12BN9U
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEPreferred Pharmaceuticals, Inc.5683885d-461c-4e7e-bbe8-dc231d7061922026-03-19Warnings, Adverse reactionsExact identifier
rxcui: 848176
unii: 826Y60901U
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEPreferred Pharmaceuticals, Inc.54eff1fc-c611-4929-bb44-c1834c08f5062026-03-19Warnings, Adverse reactionsExact identifier
application number: ANDA076543
ndc (package): 68788-7670-5
ndc (product): 68788-7670
rxcui: 848176
spl id: a34fcd1d-7b6b-451e-bdc0-1c4dd75cfb38
spl set id: 54eff1fc-c611-4929-bb44-c1834c08f506
unii: 826Y60901U

Reported adverse events (FAERS/openFDA)#

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