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 |
|---|---|---|---|---|---|---|
| Saline Laxative Cherry Laxative | SODIUM PHOSPHATE, DIBASIC AND SODIUM PHOSPHATE, MONOBASIC, UNSPECIFIED FORM | Dolgencorp Inc. | ca3c00d9-4301-4de8-94f5-34f1bcc761ab | 2017-04-13 | Warnings | 3980JIH2SW |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| CVS Health Original SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | 6d58a18c-62ba-4cee-b3cc-51db746ba50e | 2016-09-14 | Warnings | 4T6H12BN9U |
| CVS Health Cherry SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | 84a621fe-890e-4c88-9f26-f013c32b52b7 | 2016-09-14 | Warnings | 4T6H12BN9U |
| CVS Health Cherry SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | bfbf0241-51a6-4d9d-bee1-741d1645037d | 2016-09-14 | Warnings | 4T6H12BN9U |
| CVS Health Original SPF 15 Lip Balm | OXYBENZONE, OCTINOXATE, PETROLATUM | CVS | e49680bd-bd61-40cf-abc8-51a1c8808726 | 2016-09-14 | Warnings | 4T6H12BN9U |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.