NDC 67351-986-55 - DYNA-HEX CHG
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
- 67351-986
- Requested NDC
- 67351-986-55
- Package NDCs from labels
- 67351-986-05, 67351-986-15, 67351-986-55, 67351-986-75
- Manufacturer
- Dairy Dynamics L.L.C.
- Effective date
- 2015-01-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Dairy Dynamics DYNA-HEX CHG Sanitizing Teat Dip | Dairy Dynamics L.L.C. | 2015-01-15 | OTC ANIMAL DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 67351-986-05 | DYNA-HEX CHG | 18.9 L in 1 PAIL | SOLUTION | 18.9 | 1 | |
| 67351-986-15 | DYNA-HEX CHG | 56.8 L in 1 DRUM | SOLUTION | 56.8 | 1 | |
| 67351-986-55 | DYNA-HEX CHG | 208.2 L in 1 DRUM | SOLUTION | 208.2 | 1 | |
| 67351-986-75 | DYNA-HEX CHG | 1041 L in 1 TANK | SOLUTION | 1041 | 1 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Hand Wipes | CHLORHEXIDINE DIGLUCONATE AND BENZETHONIUM CHLORIDE | JIANGMEN SHUIZIRUN SANITARY ARTICLES CO., LTD. | 181e5fa0-ddda-4783-a0b5-ff95bfce6b36 | 2017-10-09 | Warnings | MOR84MUD8E |
| 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 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.