NDC 51672-2013-01 - 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
- 51672-2013
- Requested NDC
- 51672-2013-01
- Package NDCs from labels
- 51672-2013-1, 51672-2013-2, 51672-2013-3, 51672-2013-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-07-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Hydrocortisone 1% with Aloe | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-07-03 | HUMAN OTC DRUG LABEL |
| Hydrocortisone with Aloe - Proficient Rx LP | Proficient Rx LP | 2024-02-01 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-2013-1 | Hydrocortisonewith Aloe | 14.2 g in 1 TUBE | CREAM | 14.2 | 5 | |
| 51672-2013-1 | Hydrocortisonewith Aloe | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-2013-2 | Hydrocortisonewith Aloe | 1 in 1 CARTON | CREAM | 1 | 5 | |
| 51672-2013-2 | Hydrocortisonewith Aloe | 28.4 g in 1 TUBE | CREAM | 28.4 | 5 | |
| 51672-2013-3 | Hydrocortisonewith Aloe | 60 g in 1 TUBE | CREAM | 60 | 5 | |
| 51672-2013-3 | Hydrocortisonewith Aloe | 1 in 1 CARTON | CREAM | 1 | 5 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-2013 | HYDROCORTISONE WITH ALOE (HYDROCORTISONE) CREAM [TARO PHAMACEUTICALS U.S.A., INC.] | 4 | Current NDC, Legacy NDC, 6 package rows | 20241222_caa2fd64-e262-4d7c-ad8a-69f506feba8c.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-2013-1 | GM - Gram | 51672-2013 | 87032096-3d1b-41ba-b158-a04ffa9cd050 | 1 | 2013-03-03 |
| 51672-2013-2 | GM - Gram | 51672-2013 | 9666b4c8-273e-4737-8c31-b2126b89b2ce | 1 | 2013-03-03 |
DailyMed Socrata Ingredients#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| ACD A | CITRIC ACID MONOHYDRATE, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE | Terumo BCT, Ltd | 8e255bc7-a120-460a-a32d-43931f8115de | 2026-05-21 | Warnings, Adverse reactions | 2968PHW8QP |
| LidoPro Patch | LIDOCAINE, MENTHOL, AND METHYL SALICYLATE | Preferred Pharmaceuticals Inc. | 6c9a076e-6316-427b-9ce6-c8fe2d388837 | 2026-05-21 | Warnings | M017 |
| Medi-First Capsaicin Cream | CAPSAICIN | Unifirst First Aid Corporation | 49eb807b-fa31-3d84-e063-6394a90acfcf | 2026-05-20 | Warnings | M017 |
| WHITENING SUNSCREENANTI WRINKLE | WHITENING SUNSCREENANTI WRINKLE | Shantou Oushiya Biotechnology Co.,Ltd | 524384e9-b3f8-4c13-e063-6394a90a8973 | 2026-05-20 | Warnings | 059QF0KO0R |
| Biofreeze Triple Target Roll-On | CAMPHOR, CAPSAICIN, MENTHOL | Reckitt Benckiser LLC | 5089c088-3026-233a-e063-6394a90a93b6 | 2026-05-19 | Warnings | M017 |
| Lidocaine Pain Relief Patch | LIDOCAINE | GERI-CARE PHARMACEUTICAL CORP | 522f1521-f9f2-4c26-e063-6394a90a9e05 | 2026-05-19 | Warnings | M017 |
| Easment 0.1% Capsaicin Roll on | CAPSAICIN 0.1% | Easment LLC | 521212d6-57fd-4a7a-e063-6294a90a2a18 | 2026-05-18 | Warnings | M017 |
| Burn Relief | LIDOCAINE | WALMART INC. | 15af4557-4baf-c177-e063-6294a90a7a5b | 2026-05-18 | Warnings | M017 |
| Blistex Maximum Hydration Lip | CAMPHOR (SYNTHETIC), DIMETHICONE, UNSPECIFIED, MENTHOL, UNSPECIFIED FORM, AND PHENOL | Blistex Inc. | fed223bc-edf3-46eb-b678-acb906f9ef11 | 2026-05-18 | Warnings | M017 |
| Tiger Balm | CAMPHOR (SYNTHETIC), MENTHOL, AND CAPSICUM | Haw Par Healthcare Ltd. | 5066dc10-e4d5-49e9-9a5f-0ac220cfbf28 | 2026-05-18 | Warnings | M017 |
| Deep Blue Mini | MENTHOL | doTERRA International, LLC | 51dd58a8-1fd5-9cd7-e063-6394a90a1f72 | 2026-05-15 | Warnings | M017 |
| Biofreeze Overnight Gel | MENTHOL | Reckitt Benckiser LLC | f5c8c08b-c7c0-f84d-e053-2a95a90add15 | 2026-05-15 | Warnings | M017 |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 00bba5d2-b0e0-701c-e063-6294a90a5741 | 2026-05-15 | Warnings | M017 |
| Biofreeze Overnight Roll-on | MENTHOL | Reckitt Benckiser LLC | f67d7b7a-8922-73f6-e053-2995a90a2e80 | 2026-05-15 | Warnings | M017 |
| Biofreeze Overnight Relief | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 07be6e88-1850-4d6a-946d-f03830b8c4a2 | 2026-05-15 | Warnings | M017 |
| Biofreeze Roll-On and Overnight Roll-On | MENTHOL | Reckitt Benckiser LLC | 4d3dcb8f-2075-6bbc-e063-6394a90a4992 | 2026-05-15 | Warnings | M017 |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | 6bef9ccb-7a5a-4c67-b1bc-a92b167312da | 2026-05-15 | Warnings | M017 |
| Biofreeze Roll-On | MENTHOL | Reckitt Benckiser LLC | ebbbe9cb-b1ce-4dac-9fca-f54a2470c4fb | 2026-05-15 | Warnings | M017 |
| Biofreeze Precision Relief Pen | MENTHOL | Reckitt Benckiser LLC | b4cc1db5-a33f-17bc-e053-2995a90ab7eb | 2026-05-15 | Warnings | M017 |
| Biofreeze Professional | MENTHOL, UNSPECIFIED FORM | Reckitt Benckiser LLC | db982baf-31ea-4f09-90e3-cd5facb5dfe5 | 2026-05-15 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.