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 2 of 43 · 859 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HemorrhoidalGLYCERIN, PHENYLEPHRINE HCL, PRAMOXINE HCL, WHITE PETROLATUMCVS Pharmacy3167c918-a7d3-46a1-a85b-64f9c22916f22026-09-04WarningsExact identifier
unii: 4T6H12BN9U
Petroleum Skin ProtectantWHITE PETROLATUMYour Military Exchanges1a0aed14-8606-4676-b4b5-23dd415d43ac2026-09-02Warnings, Adverse reactionsExact identifier
unii: 4T6H12BN9U
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEREMEDYREPACK INC.7cacf0ec-3db9-48be-9a76-93ed4a1f042c2026-08-31Adverse reactionsExact identifier
unii: 826Y60901U
PURE PETROLATUMPETROLATUMVASA COSMETICS PRIVATE LIMITED5a57b197-3e18-b3ab-e063-6394a90aed822026-08-31WarningsExact identifier
unii: 4T6H12BN9U
HYDROPHORHYDROPHORAkron Pharma Inc.e6099df7-d418-479a-9d2e-ced523585aed2026-08-28WarningsExact identifier
unii: 4T6H12BN9U
KUGIG ALOE FOAMING INTIMATE WASHINTIMATE CLEANSING FOAMHong Kong KangXing Centennial Management Limited59f4d398-1186-a168-e063-6294a90ab44b2026-08-26WarningsExact identifier
unii: 059QF0KO0R
Sterile WaterWATERREMEDYREPACK INC.5dd5d148-6e23-41de-bff5-551b2aea95982026-08-24Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Betamethasone DipropionateBETAMETHASONE DIPROPIONATEE. Fougera & Co. a division of Fougera Pharmaceuticals, LLC97dde5f5-a865-4af2-b562-8da72c8475f32026-08-21Adverse reactionsExact identifier
unii: 826Y60901U
Rohto Optic GlowNAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOLThe Mentholatum Companydf9c5f7c-96e6-4b2b-b8cb-21a6a3342dff2026-08-20WarningsExact identifier
unii: 6DC9Q167V3
Rohto Preservative Free Dry AidPOVIDONE, PROPYLENE GLYCOLThe Mentholatum Companyf4b1974c-2412-45f6-b79d-88b8a0bcb6082026-08-18WarningsExact identifier
unii: 6DC9Q167V3
Rohto Dry-AidPOVIDONE, PROPYLENE GLYCOLThe Mentholatum Company8ea5c6c9-48f4-406a-a2cb-9280c546d87d2026-08-18WarningsExact identifier
unii: 6DC9Q167V3
BM BM63 DROPSCEANOTHUS, KALI ARSEN, KALI MUR, SELENIUM, THALLIUM, WIESBADENBM Private Limited59006d82-610a-2e08-e063-6394a90af1ed2026-08-14WarningsExact identifier
unii: 059QF0KO0R
SYSTANE HYDRATION PF PRESERVATIVE FREEPOLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOLAlcon Laboratories, Inc.8936f66f-10fe-44ab-a26e-dd8b05dfa9972026-08-10WarningsExact identifier
unii: 6DC9Q167V3
Systane Pro PFPROPYLENE GLYCOLAlcon Laboratories, Inc.23b3515f-fbe5-4398-b2df-8b2eccdd01e22026-08-10WarningsExact identifier
unii: 6DC9Q167V3
Sterile WaterWATERCardinal Health 107, LLC48d75a7c-8329-48a8-bea0-a8c144ddf6372026-08-07Warnings, Adverse reactionsExact identifier
unii: 059QF0KO0R
Petroleum Jelly, Lil Drug StorePETROLATUM JELLYLil' Drug Store Products, Inc.5862af40-97e2-d792-e063-6394a90a0f1a2026-08-06WarningsExact identifier
unii: 4T6H12BN9U
Dealmed Vitamins A and DPETROLATUMDealmed Medical Supplies, LLC.84afe4ae-f9e8-406f-9fbe-f413975f86eb2026-08-05WarningsExact identifier
unii: 4T6H12BN9U
Leader Lubricant Eye Drops 30ctPOLYETHYLENE GLYCOL 400, PROPYLENE GLYCOLCARDINAL HEALTH 110, LLC. DBA LEADER8df69f2c-40c4-245c-e053-2a95a90a54062026-08-05WarningsExact identifier
unii: 6DC9Q167V3
Petroleum JellyPETROLATUMWalgreens1bb250ee-c4b7-4e9f-9d13-46ef9df4a9f52026-08-04WarningsExact identifier
unii: 4T6H12BN9U
PROCURE VITAMIN A AND D Skin ProtectantPETROLATUMTWIN MED, LLCbbbca68e-1b65-49b1-a5fa-ed4da55d05e32026-08-03WarningsExact identifier
unii: 4T6H12BN9U

Reported adverse events (FAERS/openFDA)#

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