NDC11 43742169501
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 43742-1695-01 | 43742-1695 |
| 43742-1695-1 | 43742-1695 |
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 |
|---|---|---|---|---|---|---|
| Respiratory Plus | RIBES NIGRUM, VIBURNUM OPULUS, QUEBRACHO, BLATTA ORIENTALIS, POTHOS FOETIDUS, CINNAMIC ACID, GALLICUM ACIDUM, INDOLUM, QUERCETIN, RUTIN, ARSENICUM IODATUM, NAPHTHALINUM, COUMARINUM, OXYGENIUM, HOUSE DUST MITE, MALVIN | Deseret Biologicals, Inc. | aab86cff-ff9a-4282-9699-c8ea2c208fea | 2024-08-20 | Warnings | 43742-1695-1 43742-1695 43742169501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.