NDC 70242-121 - SUEROLYTE Oral Electrolyte Solution Pineapple Flavor
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
- 70242-121
- Package NDCs from labels
- 70242-121-33
- Manufacturer
- Dannso Corp./d.b.a. Essential Products | Alfa Vitamins Laboratories Inc
- Effective date
- 2015-08-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SUEROLYTE Oral Electrolyte Solution Pineapple Flavor | Dannso Corp./d.b.a. Essential Products | Alfa Vitamins Laboratories Inc | 2015-08-14 | DIETARY SUPPLEMENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70242-121-33 | SUEROLYTE Oral Electrolyte Solution Pineapple Flavor | 1 L in 1 BOTTLE | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70242-121 | SUEROLYTE ORAL ELECTROLYTE SOLUTION PINEAPPLE FLAVOR ( DEXTROSE, CITRIC ACID, POTASSIUM CITRATE, SODIUM CHLORIDE,SODIUM CITRATE, SUCRALOSE, ACESULFAME POTASSIUM, ZINC GLUCONATE, POTASSIUM SORBATE) LIQUID [DANNSO CORP./D.B.A. ESSENTIAL PRODUCTS] | 1 | 1 package rows | 20160530_abaae728-8c07-4b00-8abe-71aa1a4ef514.zip |
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 |
|---|---|---|---|---|---|---|
| Lactated Ringers | SODIUM CHLORIDE, SODIUM LACTATE, POTASSIUM CHLORIDE, CALCIUM CHLORIDE | Baxter Healthcare Corporation | f09f80bf-2f8b-4420-865d-aec2d5e5cd4d | 2012-06-12 | 451W47IQ8X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.