NDC 60282-2200 - Dairyland Brand Iodine Teat Dip Controlled
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
- 60282-2200
- Package NDCs from labels
- 60282-2200-1, 60282-2200-2, 60282-2200-3, 60282-2200-4
- Manufacturer
- Stearns Packaging Corporation | Lab Express International
- Effective date
- 2024-12-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| IODINE - Stearns Packaging Corporation | Lab Express International | Stearns Packaging Corporation | Lab Express International | 2024-12-17 | OTC ANIMAL DRUG LABEL |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 60282-2200 | DAIRYLAND BRAND IODINE TEAT DIP CONTROLLED (IODINE) LIQUID [STEARNS PACKAGING CORPORATION] | 5 | Unmatched | 20241219_0d896b22-19c5-4fc1-b9e8-d1db2c8b7089.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| IODINE | ACTIVE INGREDIENT | 9679TC07X4 | DAIRYLAND BRAND IODINE TEAT DIP CONTROLLED (IODINE) LIQUID [STEARNS PACKAGING CORPORATION] | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | DAIRYLAND BRAND IODINE TEAT DIP CONTROLLED (IODINE) LIQUID [STEARNS PACKAGING CORPORATION] | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | DAIRYLAND BRAND IODINE TEAT DIP CONTROLLED (IODINE) LIQUID [STEARNS PACKAGING CORPORATION] | 1 | |
| LANOLIN | INACTIVE INGREDIENT | 7EV65EAW6H | DAIRYLAND BRAND IODINE TEAT DIP CONTROLLED (IODINE) LIQUID [STEARNS PACKAGING CORPORATION] | 1 |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.