NDC 71276-140-01 - HYALURON 3S SERUM
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
- 71276-140
- Requested NDC
- 71276-140-01
- Package NDCs from labels
- 71276-140-01, 71276-140-02
- Manufacturer
- ULAB | U-LAB Switzerland AG
- Effective date
- 2017-03-22
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| HYALURON 3S SERUM - ULAB | U-LAB Switzerland AG | ULAB | U-LAB Switzerland AG | 2017-03-22 | HUMAN OTC DRUG LABEL |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 71276-140-02 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-d2b0-f424-e053-dadaa90a57ce | 9b2c77cd-31e8-45ec-8082-77682dd97a5d |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71276-140-01 | HYALURON 3S SERUM | 50 mL in 1 BOTTLE, PUMP | CREAM | 50 | 2 | |
| 71276-140-02 | HYALURON 3S SERUM | 1 in 1 CARTON | CREAM | 1 | 2 |
DailyMed Dashboard NDC Coverage#
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 |
| 3343cda2-e52d-4013-afed-601459a29267 | 9b2c77cd-31e8-45ec-8082-77682dd97a5d | 2017-03-22 | Warnings | 3343cda2-e52d-4013-afed-601459a29267 9b2c77cd-31e8-45ec-8082-77682dd97a5d | ||
| 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.