NDC 80714-034-01 - CLOROX Hand sanitizer Gel
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
- 80714-034
- Requested NDC
- 80714-034-01
- Package NDCs from labels
- 80714-034-01, 80714-034-03, 80714-034-08, 80714-034-05, 80714-034-06, 80714-034-09, 80714-034-10, 80714-034-11, 80714-034-02, 80714-034-04
- Manufacturer
- New Wave Global Services Inc
- Effective date
- 2023-12-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| CLOROX Hand sanitizer Gel - New Wave Global Services Inc | New Wave Global Services Inc | 2023-12-27 | HUMAN OTC DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Sterile Water | WATER | Baxter Healthcare Company | 210dc9ab-d6ca-4552-ac19-1be17792d290 | 2016-05-31 | Warnings, Adverse reactions | 059QF0KO0R |
| CVS Hand Sanitizer | ALCOHOL | CVS | d0081c50-c0d2-436a-ba83-5d1982ae64b7 | 2015-08-17 | Warnings | 3K9958V90M |
| Instant Hand Sanitizer | ALCOHOL | Safetec of America, Inc. | f9e30645-491b-4f54-acfd-f863ee235607 | 2013-08-07 | Warnings | 3K9958V90M |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.