NDC 21749-033 - GOJO Antibacterial Foam Sp
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
- 21749-033
- Package NDCs from labels
- 21749-033-89, 21749-033-97
- Manufacturer
- GOJO Industries, Inc.
- Effective date
- 2018-11-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| GOJO Antibacterial Foam Soap | GOJO Industries, Inc. | 2018-11-19 | 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 |
|---|---|---|---|---|---|---|
| Food Additives | BERBERIS VULGARIS, CHELIDONIUM MAJUS, TRIFOLIUM PRATENSE, GLYCYRRHIZA GLABRA, LAPPA MAJOR, PHYTOLACCA DECANDRA, RHAMNUS FRANGULA, RHAMNUS PURSHIANA, STILLINGIA SYLVATICA, XANTHOXYLUM FRAXINEUM, ARSENICUM ALBUM, BELLADONNA, LYCOPODIUM CLAVATUM, NATRUM SULPHURICUM, PHOSPHORICUM ACIDUM | BioActive Nutritional, Inc. | bf27d457-12e1-4ab6-b132-1b65cde0ed93 | 2016-09-28 | Warnings | 0YPR65R21J |
| 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.