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 | Type |
|---|---|---|---|
| Hydrocortisone Cream 1% with Aloe | NuCare Pharmaceuticals, Inc. | 2026-06-24 | HUMAN OTC DRUG LABEL |
| Hydrocortisone Cream 1% with Aloe | Sun Pharmaceutical Industries, Inc. | GOPALDAS VISRAM AND COMPANY LIMITED | 2025-06-16 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-5330-1 | Hydrocortisonewith Aloe | 1 in 1 CARTON | CREAM | 1 | 2 | |
| 51672-5330-1 | Hydrocortisonewith Aloe | 14.2 g in 1 TUBE | CREAM | 14.2 | 2 | |
| 51672-5330-2 | Hydrocortisonewith Aloe | 28.4 g in 1 TUBE | CREAM | 28.4 | 2 | |
| 51672-5330-2 | Hydrocortisonewith Aloe | 1 in 1 CARTON | CREAM | 1 | 2 | |
| 51672-5330-3 | Hydrocortisonewith Aloe | 1 in 1 CARTON | CREAM | 1 | 2 | |
| 51672-5330-3 | Hydrocortisonewith Aloe | 60 g in 1 TUBE | CREAM | 60 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-5330 | HYDROCORTISONE WITH ALOE (HYDROCORTISONE CREAM 1%) CREAM [TARO PHAMACEUTICALS U.S.A., INC.] | 1 | Current NDC, 6 package rows | 20250331_312ddc8d-100e-cfac-e063-6294a90acd09.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-5330-1 | GM - Gram | 51672-5330 | d55a9c62-93c2-4ea1-85c7-9f017497becd | 1 | 2025-05-14 |
| 51672-5330-2 | GM - Gram | 51672-5330 | 584276fc-3edd-421b-b681-8eee6e7b2ac1 | 1 | 2025-05-14 |
| 51672-5330-3 | GM - Gram | 51672-5330 | 1521f1f7-8a24-48ed-8928-eceea98c6882 | 1 | 2026-02-05 |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| A and E Marathon Delay Serum | DELAY SERUM | Phe Inc | 4355d1d8-44fe-aca1-e063-6294a90a85ff | 2025-11-11 | Warnings | M017 |
| A and E Deep Throat Desensitizing SprayStrawberry | ORAL NUMBING SPRAY STRAWBERRY | Phe Inc | 4355dab1-a293-ded6-e063-6394a90af9b0 | 2025-11-11 | Warnings | M017 |
| A and E Easy Anal Gel | ANAL NUMBING LUBRICANT | Phe Inc | 4355e0f3-65ba-eca6-e063-6394a90ab43c | 2025-11-11 | Warnings | M017 |
| A and E Deep Throat Desensitizing SprayPeppermint | ORAL NUMBING SPRAY MINT | Phe Inc | 4355e0d0-1222-d594-e063-6294a90abb29 | 2025-11-11 | Warnings | M017 |
| DermaNumb Analgesic | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 0ea46890-45c3-4732-bc47-227f7c67daf1 | 2025-11-11 | Warnings | M017 |
| Derma Numb Pain Relief | LIDOCAINE HCL | A.T.S. Laboratories, LLC | 710991ae-8f82-4893-93a7-0ef3f815d132 | 2025-11-11 | Warnings | M017 |
| HYDROCORTISONE | HYDROCORTISONE | Encube Ethicals, Inc. | 969cd576-82d3-4662-bbc1-3587a1f6a564 | 2025-11-10 | Warnings | M017 106258 WI4X0X7BPJ |
| Jelcaine Sterile | LIDOCAINE HCL JELLY USP, 2% | Brookfield Pharmaceuticals, LLC | 1a39d1de-7aa2-3068-e063-6394a90aed85 | 2025-11-10 | Warnings | M017 |
| Hush Anesthetic | LIDOCAINE | HUSH Anesthetic | c6e86a0f-6f9b-45b7-86ce-0bb1c198061a | 2025-11-10 | Warnings | M017 |
| Hush Anesthetic | LIDOCAINE | HUSH Anesthetic | 97ae1993-7268-4b7f-92e2-6004337d5650 | 2025-11-10 | Warnings | M017 |
| MENTHOL AND METHYL SALICYLATE | ELECTRIC MEDICATED BALM ULTRA STRENGTH | FEI FAH MEDICAL MANUFACTURING PTE LTD | 91e6d3b9-25bb-4015-9d96-bd27f93e5ada | 2025-11-10 | Warnings | M017 |
| E MEI SHAN MEDICATED | CAMPHOR, MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | bda1e7c1-42df-4126-a512-80f843b07fd0 | 2025-11-10 | Warnings | M017 |
| EXTRA STRENGTH HUA TUO PAIN RELIEVING | CAMPHOR AND MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | 9850754b-ac94-4ec6-b75a-8096e5ac9456 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| TONG FENG DING PAIN RELIEF | CAMPHOR AND MENTHOL | Zhejiang Dingtai Pharmaceutical Co., Ltd | fe87b864-b3ee-4a4b-8e5a-e1ee6493de0d | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Solstice Pain Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 5ef90782-8201-47d1-b57f-f032d4c9b06a | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Solstice Pain Relieving | CAMPHOR, MENTHOL, METHYL SALICYLATE | MADISON ONE ACME INC | 1388ab3a-c26f-427d-898d-0d88411a5fba | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Solstice Capsaicin Patch Hot | CAPSAICIN | MADISON ONE ACME INC | f74db6e0-853a-4eb3-a4b5-9da2cd3d95cf | 2025-11-10 | Warnings, Adverse reactions | M017 |
| Lung Choy Shung Pain Relief Liquid | MENTHOL AND CAMPHOR | MADISON ONE ACME INC | 4842c6ec-7823-4f6b-afc4-258fce2c2391 | 2025-11-10 | Warnings, Adverse reactions | M017 |
| 701 DIEDA ZHENGTONG YAOGAO MEDICATED | CAMPHOR AND MENTHOL | MADISON ONE ACME INC | 115041ff-5046-4ca4-b54b-5652037e74bd | 2025-11-10 | Warnings, Adverse reactions | M017 |
| EXTRA STRENGTH HUA TUO PAIN RELIEF | CAMPHOR AND MENTHOL | MADISON ONE ACME INC | 0f269a41-4b56-4e22-b9cb-17d99bf76a57 | 2025-11-10 | Warnings, Adverse reactions | M017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.