NDC 43406-106-01
This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
- Requested NDC
- 43406-106-01
- Product root
- 43406-106
- Identity scope
- Package
- Primary current NDC product row
- Not present
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded package | package | 43406-0106 | 43406-0106-1 | E | Excluded after deficient or non-compliant submission was not corrected | excluded / ndc_excluded.zip | 110d247fa046… | a55b01930146… |
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 |
|---|---|---|---|---|---|---|
| ALLERGY NEW ENGLAND MIX | BETULA PUBESCENS BARK, ARTEMISIA VULGARIS POLLEN, PLANTAGO LANCEOLATA POLLEN, ACER PSEUDOPLATANUS POLLEN, BETULA PUBESCENS BARK, EVERNIA PRUNASTRI BARK, ARMARANTHUS RETROFLEXUS POLLEN, PINUS MASSONIANA POLLEN, TABULIFORMIS POLLEN, AMBROSIA ARTEMISIFOLIA POLLEN, | Natural Creations, Inc. | b12b20c3-a7bf-4366-89da-a8023204048e | 2025-11-13 | Warnings | 43406010601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.