NDC 0010-4720-02 - Dry-Clox
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
- 0010-4720
- Requested NDC
- 0010-4720-02
- Package NDCs from labels
- 0010-4720-01, 0010-4720-02, 0010-4720-03
- Manufacturer
- Boehringer Ingelheim Animal Health USA Inc.
- Effective date
- 2022-05-18
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dry-Clox - Boehringer Ingelheim Animal Health USA Inc. | Boehringer Ingelheim Animal Health USA Inc. | 2022-05-18 | PRESCRIPTION ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0010-4720-01 | Dry-Clox | 10 mL in 1 SYRINGE | GEL | 10 | 11 | |
| 0010-4720-02 | Dry-Clox | 12 in 1 CARTON | GEL | 12 | 11 | |
| 0010-4720-03 | Dry-Clox | 144 in 1 PAIL | GEL | 144 | 11 |
DailyMed Dashboard NDC Coverage#
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CLOXACILLIN BENZATHINE | ACTIVE INGREDIENT | AC79L7PV2G | DRY-CLOX (CLOXACILLIN BENZATHINE) GEL [BOEHRINGER INGELHEIM VETMEDICA, INC] | 6 | |
| CLOXACILLIN | ACTIVE MOIETY | O6X5QGC2VB | DRY-CLOX (CLOXACILLIN BENZATHINE) GEL [BOEHRINGER INGELHEIM VETMEDICA, INC] | 6 |
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.
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| Wasted | BENZALKONIUM CHLORIDE | Freshorize Ltd | 0c43b516-7608-c826-e063-6294a90ae4e3 | 2025-10-23 | Warnings | ZF94AP8MEY |
| Anubis Barcelona Vital Line | HYDROLYZED COLLAGEN | ANUBIS COSMETICS SL | f564bbf0-3b5c-4a81-e053-2a95a90a7ea6 | 2023-08-29 | Warnings | ZF94AP8MEY |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.