NDC 51672-1275-01 - Clotrimazole
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
- 51672-1275
- Requested NDC
- 51672-1275-01
- Package NDCs from labels
- 51672-1275-1, 51672-1275-2, 51672-1275-6, 51672-1275-7, 51672-1275-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc.
- Effective date
- 2025-09-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Clotrimazole Cream USP, 1% | Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | 2025-09-10 | HUMAN PRESCRIPTION DRUG LABEL |
| Clotrimazole Cream USP, 1% | REMEDYREPACK INC. | 2024-03-15 | HUMAN PRESCRIPTION DRUG LABEL |
| Clotrimazole - A-S Medication Solutions | A-S Medication Solutions | 2023-11-22 | HUMAN PRESCRIPTION DRUG LABEL |
| Clotrimazole - Proficient Rx LP | Proficient Rx LP | 2022-02-01 | HUMAN PRESCRIPTION DRUG LABEL |
| Clotrimazole Cream USP, 1% | NuCare Pharmaceuticals,Inc. | 2022-01-14 | HUMAN PRESCRIPTION DRUG LABEL |
| Clotrimazole Cream USP, 1% | NuCare Pharmaceuticals,Inc. | 2021-07-06 | HUMAN PRESCRIPTION DRUG LABEL |
| Clotrimazole - Physicians Total Care, Inc. | Physicians Total Care, Inc. | 2011-03-16 | HUMAN OTC DRUG LABEL |
| CLOTRIMAZOLE - STAT RX USA LLC | STAT RX USA LLC | 2010-08-02 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-1275-1 | Clotrimazole | 1 in 1 CARTON | CREAM | 1 | 8 | |
| 51672-1275-1 | Clotrimazole | 15 g in 1 TUBE | CREAM | 15 | 8 | |
| 51672-1275-2 | Clotrimazole | 1 in 1 CARTON | CREAM | 1 | 8 | |
| 51672-1275-2 | Clotrimazole | 30 g in 1 TUBE | CREAM | 30 | 8 | |
| 51672-1275-6 | Clotrimazole | 45 g in 1 TUBE | CREAM | 45 | 8 | |
| 51672-1275-6 | Clotrimazole | 1 in 1 CARTON | CREAM | 1 | 8 | |
| 51672-1275-7 | Clotrimazole | 45 g in 1 TUBE | CREAM | 45 | 8 | |
| 51672-1275-7 | Clotrimazole | 2 in 1 CARTON | CREAM | 2 | 8 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 51672-1275 | CLOTRIMAZOLE CREAM [TARO PHARMACEUTICALS U.S.A., INC.] | 5 | Current NDC, Legacy NDC, 8 package rows | 20241222_77883cfd-f13c-40cb-88b2-8f777e1cdce9.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 51672-1275-1 | GM - Gram | 51672-1275 | 593d29e0-4cba-46cc-a57d-5c9bf5e95293 | 1 | 2012-07-24 |
| 51672-1275-2 | GM - Gram | 51672-1275 | e0172989-2c5a-4d8c-a2f9-4fa2ab03afe3 | 1 | 2012-07-24 |
| 51672-1275-6 | GM - Gram | 51672-1275 | 18918d69-9395-4a2e-a101-5f77f5ef6fec | 1 | 2012-07-24 |
| 51672-1275-7 | GM - Gram | 51672-1275 | 1c0757eb-637f-4136-b40b-c8282abd88ea | 1 | 2012-07-24 |
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 |
|---|---|---|---|---|---|---|
| Clotrimazole and Betamethasone Dipropionate | CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE | Proficient Rx LP | c6e4bf5f-f6d6-489e-9286-c30568c601b7 | 2021-01-01 | Warnings, Adverse reactions | G07GZ97H65 |
| Clotrimazole and Betamethasone Dipropionate | CLOTRIMAZOLE AND BETAMETHASONE DIPROPIONATE | Glenmark Pharmaceuticals Inc. USA | 8dcd24cb-e568-428a-88ac-737d115cc54d | 2020-11-09 | Warnings, Adverse reactions | G07GZ97H65 |
| Clotrimazole | CLOTRIMAZOLE TOPICAL | Novitium Pharma LLC | 02df90b9-4879-4e73-b03a-0e96f3d099ea | 2020-08-13 | Warnings, Adverse reactions | G07GZ97H65 |
| Bach Original Flower Remedies | WATER | Nelson Bach USA Limited | 09c76050-42c5-4403-865c-a1f6f668d9c0 | 2020-06-15 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 8bcf5572-49e1-4302-9522-56f57904cb4a | 2019-12-29 | Warnings, Adverse reactions | 059QF0KO0R |
| Dynamic Eyewash with Eyecup | WATER | Dynamic Safety International | 7d3af0f4-0e1f-9ea5-e053-2991aa0af7a2 | 2018-12-17 | Warnings | 059QF0KO0R |
| Bio Rock Water | ROCK WATER | BioActive Nutritional, Inc. | 178bd16d-0d4f-49d8-866b-8ab3a3c6889d | 2018-07-30 | Warnings | 059QF0KO0R |
| Ivy-Dry Super | BENZYL ALCOHOL, CAMPHOR, MENTHOL | Ivy-Dry, Inc. | 4792a667-2378-4b3d-968d-9efb1866792f | 2017-12-27 | Warnings | LKG8494WBH |
| Homeoplex D | GLYCERINUM, PHYTOLACCA DECANDRA, TARAXACUM OFFICINALE, ARSENICUM ALBUM, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PHOSPHORUS, ACETYLSALICYLICUM ACIDUM, GLONOINUM, INSULINUM (SUIS), LITHIUM CARBONICUM, THYROIDINUM (SUIS), SALICYLICUM ACIDUM, ADRENOCORTICOTROPHIN, CORTISONE ACETICUM, EUGENOL, STEARYL ALCOHOL, XYLITOL, FOLLICULINUM, BENZOICUM ACIDUM, CHLORINUM, POTASSIUM SORBATE, SORBITOL, RESORCINUM, BENZYL ALCOHOL, LACTICUM ACIDUM, ISOPROPYL PALMITATE, BORICUM ACIDUM, ACETICUM ACIDUM, | Supplement Clinic, LLC. | cd6b48ab-3566-484d-8deb-15ef6f8e7e8f | 2017-11-01 | Warnings | LKG8494WBH |
| Sterile Water | WATER | Baxter Healthcare Corporation | ef3e79c5-3f58-4b36-a296-64b7d9a651c1 | 2017-10-17 | Warnings, Adverse reactions | 059QF0KO0R |
| Eye Wash | WATER | CVS Pharmacy | 049cee29-7ec2-4d5b-8308-f522acde43a7 | 2017-03-29 | Warnings | 059QF0KO0R |
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| e58a7f34-4791-4ebb-b13a-75caf23f0f8d | 1fa2664f-955d-4ae1-85ff-186e4aebba49 | 2011-03-16 | Warnings, Adverse reactions | e58a7f34-4791-4ebb-b13a-75caf23f0f8d 1fa2664f-955d-4ae1-85ff-186e4aebba49 | ||
| 82a3de99-961a-4554-9a86-5b94b4304b5a | f003ee1a-a7f6-46b4-8ca7-60bc2ce732f6 | 2010-08-02 | Warnings, Adverse reactions | 82a3de99-961a-4554-9a86-5b94b4304b5a f003ee1a-a7f6-46b4-8ca7-60bc2ce732f6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.