NDC 84778-112 - Salkalli
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
- 84778-112
- Package NDCs from labels
- 84778-112-01, 84778-112-02, 84778-112-03, 84778-112-04
- Manufacturer
- Guangzhou Yixin Cross-border E-commerce Co., Ltd.
- Effective date
- 2025-11-07
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Salkalli - Guangzhou Yixin Cross-border E-commerce Co., Ltd. | Guangzhou Yixin Cross-border E-commerce Co., Ltd. | 2025-11-07 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 84778-112-01 | Salkalli | 3 mL in 1 SYRINGE | INJECTION, SOLUTION | 3 | 1 | |
| 84778-112-01 | Salkalli | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | 1 | |
| 84778-112-02 | Salkalli | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | 1 | |
| 84778-112-02 | Salkalli | 2 in 1 PACKAGE, COMBINATION | INJECTION, SOLUTION | 2 | 1 | |
| 84778-112-03 | Salkalli | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | 1 | |
| 84778-112-03 | Salkalli | 3 in 1 PACKAGE, COMBINATION | INJECTION, SOLUTION | 3 | 1 | |
| 84778-112-04 | Salkalli | 4 in 1 PACKAGE, COMBINATION | INJECTION, SOLUTION | 4 | 1 | |
| 84778-112-04 | Salkalli | 1 in 1 CARTON | INJECTION, SOLUTION | 1 | 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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 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.