NDC 70710-1233-01 - 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
- 70710-1233
- Requested NDC
- 70710-1233-01
- Package NDCs from labels
- 70710-1233-1, 70710-1233-4, 70710-1233-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2025-07-25
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Betamethasone dipropionate - REMEDYREPACK INC. | REMEDYREPACK INC. | 2025-07-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Betamethasone dipropionate - A-S Medication Solutions | A-S Medication Solutions | 2023-12-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Betamethasone dipropionate - A-S Medication Solutions | A-S Medication Solutions | 2023-10-31 | HUMAN PRESCRIPTION DRUG LABEL |
| BETAMETHASONE - Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | Zydus Pharmaceuticals USA Inc. | Zydus Lifesciences Limited | 2022-10-05 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70710-1233-1 | Betamethasone dipropionate | 15 g in 1 TUBE | CREAM | 15 | 3 | |
| 70710-1233-1 | Betamethasone dipropionate | 1 in 1 CARTON | CREAM | 1 | 3 | |
| 70710-1233-4 | Betamethasone dipropionate | 1 in 1 CARTON | CREAM | 1 | 3 | |
| 70710-1233-4 | Betamethasone dipropionate | 45 g in 1 TUBE | CREAM | 45 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70710-1233 | BETAMETHASONE DIPROPIONATE CREAM [ZYDUS PHARMACEUTICALS USA INC.] | 3 | Current NDC, Legacy NDC, 4 package rows | 20221007_18d80661-72ad-4a83-917f-a80ce37a5568.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 70710-1233-1 | GM - Gram | 70710-1233 | 76e92d62-4588-4356-b5ae-513a2a3f2635 | 1 | 2019-05-02 |
| 70710-1233-4 | GM - Gram | 70710-1233 | ae208291-c0e1-424c-a37c-ce2ac84eac86 | 1 | 2019-05-02 |
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 D plus E | VITAMIN A, D AND E OINTMENT | Derma Sciences Canada Inc. | 35aca592-bfd0-652f-e063-6394a90ac53e | 2025-07-22 | Warnings | 4T6H12BN9U |
| Petroleum Jelly | PETROLATUM | Derma Sciences Canada Inc. | 3a895e6c-da8d-db9b-e063-6394a90ace40 | 2025-07-22 | Warnings | 4T6H12BN9U |
| GoodSense Hemorrhoidal Pain Relief | GLYCERIN, LIDOCAINE, PETROLATUM, PHENYLEPHRINE HCL | Perrigo Direct, Inc | 2e5f699d-45e8-6451-e063-6394a90a8ad8 | 2025-07-20 | Warnings | 4T6H12BN9U |
| Eyeleve MGD | MINERAL OIL | Bruder Healthcare | 145b66e2-00e1-410e-8539-e12ffc4f6f82 | 2025-07-15 | Warnings | T5L8T28FGP |
| Nikzon Hemorrhoidal | GLYCERIN, PETROLATUM, PHENYLEPHRINE HYDROCHLORIDE, AND PRAMOXINE HYDROCHLORIDE | Genomma Lab USA | 8f9a9939-2c99-489f-b597-9a51ec2684f9 | 2025-07-14 | Warnings | 4T6H12BN9U |
| Sterile Water | STERILE WATER | Nephron Pharmaceuticals Corporation | bc04a883-babc-87a6-e053-2995a90a3dfd | 2025-07-11 | Warnings, Adverse reactions | 059QF0KO0R |
| 5df99693-44c9-4b31-8628-26de2fff6d9d | cd94c962-86cc-4553-8063-62f51ce9f2fd | 2025-07-11 | Adverse reactions | cd94c962-86cc-4553-8063-62f51ce9f2fd | ||
| Neosporin Lip Health Overnight Renewal Therapy | PETROLATUM | Kenvue Brands LLC | 0da54fe1-c99f-4a2d-9ee5-2dc24005096c | 2025-07-10 | Warnings | 4T6H12BN9U |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | Golden State Medical Supply, Inc. | 9571a031-179d-7dfb-e053-2995a90aa016 | 2025-07-10 | Adverse reactions | 238920 826Y60901U |
| COCOA BUTTER PETROLEUM jelly | PETROLATUM | Savvy Care & Cosmetics Pvt. Ltd. | 397d13f1-3b86-3c76-e063-6394a90a0f24 | 2025-07-09 | Warnings | 4T6H12BN9U |
| Desitin Multi-Purpose Healing | PETROLATUM | Kenvue Brands LLC | 30f06dbb-de8c-43ee-b1ed-99ffd59dd3ab | 2025-07-07 | Warnings | 4T6H12BN9U |
| Clotrimazole and Betamethasone Dipropionate | CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | e4e9f244-4a85-4c0d-9917-93182c4a6e87 | 2025-07-07 | Adverse reactions | 826Y60901U |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | 3b23a3c0-3306-4a2d-932d-25916d16dc68 | 2025-07-07 | Warnings, Adverse reactions | 826Y60901U |
| Betamethasone dipropionate | BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | dc3dd2f7-38ad-4c4c-8602-29b33cc6af90 | 2025-07-07 | Warnings, Adverse reactions | 826Y60901U |
| Rexall Ready to use 4pk LAXATIVE | SODIUM PHOSPHATE, DIBASIC, UNSPECIFIED FORM AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | Dolgencorp, LLC | 78509915-0ef1-4238-99a5-78a49a68f98f | 2025-07-07 | Warnings | 3980JIH2SW |
| Creamy Petroleum | PETROLATUM | Savvy Care & Cosmetics Pvt Ltd | 3916daee-f8d2-e3f0-e063-6294a90a3883 | 2025-07-04 | Warnings | 4T6H12BN9U |
| Hemorrhoidal Cream | GLYCEROL, PHENYLEPHINE, PRAMOXINE, PETROLATUM | Trifecta Pharmaceuticals Usa Llc | 38cf4e43-280b-eb96-e063-6294a90a5949 | 2025-07-02 | Warnings | 4T6H12BN9U |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | bc12c828-54ba-411d-b752-9b735f7adf63 | 2025-07-02 | Adverse reactions | 238920 826Y60901U |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | e041ceb2-8bda-4703-b663-804e7b462e32 | 2025-07-02 | Adverse reactions | 826Y60901U |
| Calcipotriene and Betamethasone Dipropionate | CALCIPOTRIENE AND BETAMETHASONE DIPROPIONATE | Sun Pharmaceutical Industries, Inc. | 1d0ab2e6-1ab1-4d3e-ad55-7fa26446f191 | 2025-07-01 | Warnings, Adverse reactions | 826Y60901U |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.