NDC 51672-5330-01 - Hydrocortisone with Aloe

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
51672-5330
Requested NDC
51672-5330-01
Package NDCs from labels
51672-5330-1, 51672-5330-2, 51672-5330-3, 51672-5330-01
Manufacturer
NuCare Pharmaceuticals, Inc.
Effective date
2026-06-24
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Hydrocortisone Cream 1% with AloeNuCare Pharmaceuticals, Inc.2026-06-24HUMAN OTC DRUG LABEL
Hydrocortisone Cream 1% with AloeSun Pharmaceutical Industries, Inc. | GOPALDAS VISRAM AND COMPANY LIMITED2025-06-16HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51672-5330-1Hydrocortisonewith Aloe1 in 1 CARTONCREAM12
51672-5330-1Hydrocortisonewith Aloe14.2 g in 1 TUBECREAM14.22
51672-5330-2Hydrocortisonewith Aloe28.4 g in 1 TUBECREAM28.42
51672-5330-2Hydrocortisonewith Aloe1 in 1 CARTONCREAM12
51672-5330-3Hydrocortisonewith Aloe1 in 1 CARTONCREAM12
51672-5330-3Hydrocortisonewith Aloe60 g in 1 TUBECREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51672-5330HYDROCORTISONE WITH ALOE (HYDROCORTISONE CREAM 1%) CREAM [TARO PHAMACEUTICALS U.S.A., INC.]1Current NDC, 6 package rows20250331_312ddc8d-100e-cfac-e063-6294a90acd09.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-5330-1GM - Gram51672-5330d55a9c62-93c2-4ea1-85c7-9f017497becd12025-05-14
51672-5330-2GM - Gram51672-5330584276fc-3edd-421b-b681-8eee6e7b2ac112025-05-14
51672-5330-3GM - Gram51672-53301521f1f7-8a24-48ed-8928-eceea98c688212026-02-05

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 50 of 175 · 3,481 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Mineral Ice Pain RelievingMENTHOLCrown Laboratories7b30076a-0af6-2f74-e053-2a91aa0ae08d2026-01-12WarningsExact identifier
application number: M017
SarnaPRAMOXINE HYDROCHLORIDECrown Laboratories19b0ce1b-e147-01a1-e063-6394a90af8082026-01-12WarningsExact identifier
application number: M017
SarnaPRAMOXINE HYDROCHLORIDE, MENTHOLCrown Laboratories, Inc19c41e75-a654-90cf-e063-6394a90a7e972026-01-12WarningsExact identifier
application number: M017
HydrocortisoneHYDROCORTISONECrown Laboratoriesa84830ad-73dc-4a2e-b987-0a11035265352026-01-12Adverse reactionsExact identifier
rxcui: 106258
unii: WI4X0X7BPJ
AlacortHYDROCORTISONECrown Laboratoriesde000081-a245-4f6b-9e7c-e47d84b823382026-01-12Adverse reactionsExact identifier
rxcui: 106258
unii: WI4X0X7BPJ
Itch ReliefDIPHENHYDRAMINE HCL, ZINC ACETATEHY-VEE, INC48350b54-8d9a-48c4-e063-6394a90ac0402026-01-12WarningsExact identifier
application number: M017
LidoPlus Pain ReliefLIDOCAINE HYDROCHLORIDECentura Pharmaceuticals, Inc07bacc6c-60a6-4297-8663-904a22bdc0402026-01-12WarningsExact identifier
application number: M017
BlueStop MaxEXTERNAL ANALGESICClavel Corporationf1efb51c-5217-4cb2-e053-2a95a90a7f952026-01-12WarningsExact identifier
application number: M017
BlueStop MaxEXTERNAL ANALGESICClavel Corporationf2277e27-868b-57ef-e053-2a95a90abf282026-01-12WarningsExact identifier
application number: M017
Neomycin and Polymyxin B Sulfates and HydrocortisoneNEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONEREMEDYREPACK INC.04fe1b32-adfb-4c36-a986-d81b49497e0f2026-01-12Warnings, Adverse reactionsExact identifier
unii: WI4X0X7BPJ
BLT 3TETRACAINECENTURA PHARMACEUTICALS INC401a0d22-1181-02ac-e054-00144ff88e882026-01-12WarningsExact identifier
application number: M017
Sting Relief Prep PadBENZOCAINENINGBO TIANBO FIRST AID PRODUCT CO., LTD.0c901f64-6890-45c0-9ca7-ee9de87903c42026-01-12WarningsExact identifier
application number: M017
Goodsense Oral Pain ReliefBENZOCAINEGeiss, Destin and Dunn, Inc.eb461b70-d10f-4e11-8374-e43713f3504d2026-01-12WarningsExact identifier
application number: M017
Extra Strength BalmCAPSICUM AND MENTHOLSaje Natural Business Incf516e416-446b-8f21-e053-2a95a90afd882026-01-12WarningsExact identifier
application number: M017
Pain ReleaseMENTHOLSaje Natural Business Inc.3df0e56a-7651-42dc-8ed8-f68836a63c612026-01-12WarningsExact identifier
application number: M017
Trauma LessMENTHOLSaje Natural Business Inc.650cba4c-6aba-48c3-9c41-841f199055482026-01-12WarningsExact identifier
application number: M017
MamisanLIDOCAINE HYDROCHLORIDE, MENTHOLMiramar Cosmetics, Inc DBA Miramar Lab4402e900-c6e9-4f32-8cc4-c84014384a9f2026-01-12WarningsExact identifier
application number: M017
Curist Lidocaine PatchLIDOCAINE 4% PATCHLittle Pharma, Inc.1a8fe44e-7a21-c2ab-e063-6394a90a61002026-01-11WarningsExact identifier
application number: M017
DG Health Pain RelievingLIDOCAINE HCLDOLGENCORP, LLC923aeb4c-049f-4ecc-a77e-9ffa0e236d4e2026-01-11WarningsExact identifier
application number: M017
XIMONTH Nail Repairs PatchesGLYCERINShantou Ximonth Biotechnology Co., Ltd.47f1a711-5d6f-c023-e063-6294a90aa8012026-01-09WarningsExact identifier
unii: ZY81Z83H0X

Reported adverse events (FAERS/openFDA)#

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