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 |
|---|---|---|---|---|---|---|
| HUO LUO PAIN RELIEVING | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 65581716-5a2c-4ee8-816d-00caed7b95b4 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| JOSEPHS LION PAIN RELIEVING | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 69b88e21-2001-4fb2-b6eb-17f2d6e0ef2e | 2025-11-10 | Warnings, Adverse reactions | M017 |
| QIAN LI ZHUI FENG PAIN RELIEVING | CAMPHOR, MENTHOL, AND METHYL SALICYLATE | MADISON ONE ACME INC | 03a4fb7c-2328-409d-99c8-cbcf2b4a451f | 2025-11-10 | Warnings, Adverse reactions | M017 |
| WU YANG BRAND PAIN RELIEVING MEDICATED | MENTHOL AND CAMPHOR | MADISON ONE ACME INC | 05c6b95a-aeb6-4234-97c7-8d77eccb38d8 | 2025-11-10 | Warnings | M017 |
| HEI GUI PAIN RELIEVING | CAMPHOR AND METHYL SALICYLATE | MADISON ONE ACME INC | 4140c404-edab-4923-941d-f74125e943a9 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| E MEI SHAN MEDICATED | CAMPHOR AND MENTHOL | MADISON ONE ACME INC | ddcc814e-fcc4-4232-9ab4-826b8aac35f0 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Overtime | METHYL SALICYLATE, MENTHOL AND CAPSAICIN | Physicians Science & Nature Inc. | 25fec070-8587-42d1-ba6f-1a9c150acc98 | 2025-11-10 | Warnings | M017 |
| Dendracin Neurodendraxcin | METHYL SALICYLATE, MENTHOL AND CAPSAICIN | Physicians Science & Nature Inc. | 05742cd5-ece2-4007-bdf0-46b76d23df74 | 2025-11-10 | Warnings | M017 |
| Anal Blu | DESENSITIZER | Novelties by Nasswalk, Inc. | 03b9555b-c3ff-4baa-e063-6394a90afb2c | 2025-11-10 | Warnings | M017 |
| Stallion | DELAY CREME | Novelties by Nasswalk, Inc. | 0261ec88-8fe4-d5f8-e063-6294a90ab3d4 | 2025-11-10 | Warnings | M017 |
| ANAL-ESE | DESENSITIZER | Novelties by Nasswalk, Inc. | 03b89eed-b433-a263-e063-6294a90a675b | 2025-11-10 | Warnings | M017 |
| Instant Erection | ULTIMATE ERECTION ENHANCER | Novelties by Nasswalk, Inc. | 03a444f9-7052-0c38-e063-6294a90a4e56 | 2025-11-10 | Warnings | M017 |
| STA-HARD | DESENSITIZING LUBRICANT | Novelties by Nasswalk, Inc. | 02ef794b-8e70-5c26-e063-6294a90a28d1 | 2025-11-10 | Warnings | M017 |
| ANAL-ESE | DESENSITIZER | Novelties by Nasswalk, Inc. | 03a4a7ce-4cff-a608-e063-6294a90ad65d | 2025-11-10 | Warnings | M017 |
| FOOTSPA PEDI | ALCOHOL | CHEMCO CORPORATION | 04de4392-74f6-7df8-e063-6294a90ae3b1 | 2025-11-08 | Warnings | M017 |
| NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE | NEOMYCIN SULFATE, POLYMYXIN B SULFATE, HYDROCORTISONE | Amneal Pharmaceuticals NY LLC | 6fff6c70-ea1f-449c-be0c-b989de36bd67 | 2025-11-07 | Warnings, Adverse reactions | WI4X0X7BPJ |
| STERILE WATER | WATER | Henry Schein, Inc. | f4087143-9868-4308-b96c-43657ee8ec28 | 2025-11-07 | Warnings, Adverse reactions | 059QF0KO0R |
| Johnson and Johnson All Purpose First Aid Kit | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | 5cdb47c5-7951-4279-8a05-0a3199d3dd45 | 2025-11-06 | Warnings | M017 |
| Johnson and Johnson First Aid Travel Ready 80 CT | ACETAMINOPHEN, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | f388f105-48ba-4616-e053-2a95a90a0049 | 2025-11-06 | Warnings | M017 |
| Johnson and Johnson First Aid All Purpose 160 CT | ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE, ZINC ACETATE, NEOMYCIN SULFATE, POLYMYXIN B SULFATE, AND PRAMOXINE HYDROCHLORIDE | Kenvue Brands LLC | f3933330-2550-4a88-e053-2a95a90a3997 | 2025-11-06 | Warnings | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.