NDC 86000-0002 - North Country Dairy Supply TD7001N
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
- 86000-0002
- Package NDCs from labels
- 86000-0002-1, 86000-0002-2, 86000-0002-3, 86000-0002-4, 86000-0002-5, 86000-0002-6
- Manufacturer
- Surpass Chemical Co., Inc.
- Effective date
- 2014-05-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| North Country Dairy Supply TD7001N | Surpass Chemical Co., Inc. | 2014-05-12 | OTC ANIMAL DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| IODINE | ACTIVE INGREDIENT | 9679TC07X4 | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 1 | |
| IODINE | ACTIVE MOIETY | 9679TC07X4 | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 1 | |
| GLYCERIN | INACTIVE INGREDIENT | PDC6A3C0OX | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 1 | |
| ISOPROPYL ALCOHOL | INACTIVE INGREDIENT | ND2M416302 | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 1 | |
| NONOXYNOL-12 | INACTIVE INGREDIENT | 6NR43D77O6 | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 1 | |
| TRISODIUM CITRATE DIHYDRATE | INACTIVE INGREDIENT | B22547B95K | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 1 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | NORTH COUNTRY DAIRY SUPPLY TD7001N (IODINE) SOLUTION [SURPASS CHEMICAL CO., INC.] | 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.