NDC 51672-1309-01 - 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
- 51672-1309
- Requested NDC
- 51672-1309-01
- Package NDCs from labels
- 51672-1309-1, 51672-1309-3, 51672-1309-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-07-02
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Betamethasone Dipropionate Gel (Augmented*), 0.05% | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-07-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-1309-1 | Betamethasone Dipropionate | 15 g in 1 TUBE | GEL | 15 | 6 | |
| 51672-1309-1 | Betamethasone Dipropionate | 1 in 1 CARTON | GEL | 1 | 6 | |
| 51672-1309-3 | Betamethasone Dipropionate | 1 in 1 CARTON | GEL | 1 | 6 | |
| 51672-1309-3 | Betamethasone Dipropionate | 50 g in 1 TUBE | GEL | 50 | 6 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-1309 | BETAMETHASONE DIPROPIONATE GEL [TARO PHARMACEUTICALS U.S.A., INC.] | 5 | Current NDC, Legacy NDC, 4 package rows | 20241222_e041ceb2-8bda-4703-b663-804e7b462e32.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-1309-1 | GM - Gram | 51672-1309 | 8f10039b-85a5-4ecd-bcea-3bab503cd157 | 1 | 2012-07-24 |
| 51672-1309-3 | GM - Gram | 51672-1309 | aaa573ed-58dc-4041-9cbf-2a97c4d5b376 | 1 | 2012-07-24 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Betamethasone Dipropionate | ACTIVE INGREDIENT | 826Y60901U | BETAMETHASONE DIPROPIONATE GEL [TARO PHARMACEUTICALS U.S.A., INC.] | 2 | |
| Betamethasone | ACTIVE MOIETY | 9842X06Q6M | BETAMETHASONE DIPROPIONATE GEL [TARO PHARMACEUTICALS U.S.A., INC.] | 2 |
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 |
|---|---|---|---|---|---|---|
| Droptics Performance Eye Drops | NAPHAZOLINE HYDROCHLORIDE, PROPYLENE GLYCOL | Droptics LLC | 20fd6822-a7fd-4593-92bb-0a07260893e2 | 2026-02-09 | Warnings | 6DC9Q167V3 |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | A-S Medication Solutions | abd5a08c-4bb7-46c9-9e2e-0a89c43d46c8 | 2026-02-06 | Warnings, Adverse reactions | 826Y60901U |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC | 4f411e41-00dc-47cf-8517-3ff5876e1bf5 | 2026-01-30 | Warnings, Adverse reactions | 826Y60901U |
| Betamethasone Dipropionate | BETAMETHASONE DIPROPIONATE | E. Fougera & Co. a division of Fougera Pharmaceuticals, LLC | 853399f8-95a7-41f3-80e7-7ed8e3ff1a5e | 2026-01-30 | Warnings, Adverse reactions | 826Y60901U |
| INSULIN DILUTING MEDIUM FOR Kirsty | WATER | Biocon Biologics Inc. | 3db1d482-7e1f-aec6-79ef-3f305b4d8277 | 2026-01-20 | Warnings, Adverse reactions | 059QF0KO0R |
| Betamethasone Dipropionate USP, 0.05% | BETAMETHASONE DIPROPIONATE USP, 0.05% | TruPharma LLC | fc34987a-e803-4ac8-8a1e-9bdadd3f8b56 | 2026-01-18 | Adverse reactions | 826Y60901U |
| Walgreens Sterile Soothing Eye Wash | PURIFIED WATER | Walgreens | a62e3294-abd6-48dc-81b1-62a809bdc968 | 2026-01-14 | Warnings | 059QF0KO0R |
| Clotrimazole and Betamethasone Dipropionate | CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE | A-S Medication Solutions | 2eff5585-f013-42f0-b678-bb5406e8188c | 2026-01-09 | Warnings, Adverse reactions | 826Y60901U |
| Lubricant Eye Drops Solution | POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL | AvPAK | f5743b38-e3d2-a065-e053-2995a90a4b9a | 2026-01-08 | Warnings | 6DC9Q167V3 |
| Plus Rinse Emergency Eyewash | PURIFIED WATER | INNOVATIVE SAFETY SUPPLY INC. | b3f47d26-39e4-4aea-bb92-358def52b652 | 2026-01-08 | Warnings | 059QF0KO0R |
| pH Neutral Emergency Eyewash | WATER | INNOVATIVE SAFETY SUPPLY INC. | 29a1bd1e-d0dd-478f-e063-6394a90ab0aa | 2026-01-08 | Warnings | 059QF0KO0R |
| Eye Clean | EYE WASH | HART Health | 41f53e2e-c2bc-4bf1-a541-3bcb2cf63002 | 2025-12-31 | Warnings | 059QF0KO0R |
| teeth and gums | CALC FLUORICA, CALC PHOS, FERRUM PHOS, KALI PHOS, MAG PHOS, MALUS PUMILA, FLOS, ROCK WATER, ULEX EUROPAEUS, FLOS | Siddha Flower Essences LLC | 926c79d5-d270-4c0d-aca9-b58571c24f3a | 2025-12-31 | Warnings | 059QF0KO0R |
| lung and sinus | CALC PHOS, FERRUM PHOS, GENTIANELLA AMARELLA, FLOS, KALI MUR, KALI PHOS, KALI SULPH, ROCK WATER, ROSE CANINA, FLOS | Siddha Flower Essences LLC | 9f7c949f-21bc-473c-ab8d-24837893fccc | 2025-12-31 | Warnings | 059QF0KO0R |
| Signature Care Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Better Living Brands LLC | 6f1f4f58-3208-4b06-9afb-c4beeed09314 | 2025-12-30 | Warnings | 6DC9Q167V3 |
| Target Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Target Corporation | 6c449374-8847-4c4a-9073-1951ff31d404 | 2025-12-30 | Warnings | 6DC9Q167V3 |
| Target Lubricant Eye Drops High Performance | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Target Corporation | ddc15dac-fbd8-42fa-80db-79f49fc6b9eb | 2025-12-30 | Warnings | 6DC9Q167V3 |
| CVS Hydration Eye Drops | POLYETYLENE GLYCOL 400, PROPYLENE GLYCOL | CVS | ecab8fa3-6575-0dde-e053-2a95a90abd61 | 2025-12-30 | Warnings | 6DC9Q167V3 |
| GoodSense Ultra Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | Geiss, Destin & Dunn, Inc. | 9b45ebb5-c43b-c9fb-e053-2a95a90a3411 | 2025-12-30 | Warnings | 6DC9Q167V3 |
| Medics Choice Fresh and Soothe Lubricant Eye Drops | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | KC Pharmaceuticals, Inc. | 1f65b91a-4eac-65c2-e063-6394a90a0295 | 2025-12-30 | Warnings | 6DC9Q167V3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.