NDC 43406-0114-01

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: 43406-0114-01
Product root: 43406-0114
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.

Historic NDC status page 1 of 1 · 4 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Code, Status table
Captured / source date	Code	Status	Snapshot	Source SHA-256
2021-12-27 23:28 UTC · source 2021-12-27	I	Inactivated by FDA	`8dfbde2a14a4…`	`c9ff85d89658…`
2020-12-18 03:04 UTC · source 2020-12-17	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2019-12-08 06:16 UTC · source 2019-12-05	E	Excluded after deficient or non-compliant submission was not corrected	`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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
BITING INSECT ANTIGEN	APIS MELLIFERA, ARNICA MONTANA, BLATTA ORIENTALIS, DIEFFENBACHIA SEGUINE, CIMEX LECTULARIUS, CULEX PIPIENS, FORMICA RUFA, HYPERICUM PERFORATUM, LATRODECTUS MACTANS, LEDUM PALUSTRE TWIG, LOXOSCELES RECLUSA, PEDICULUS HUMANUS VAR. CAPITIS, PULEX IRRITANS, DELPHINIUM STAPHISAGRIA SEED, VESPA CRABRO.	Natural Creations, Inc.	d38e3f31-2b7a-4c25-9d80-6aa13d03b368	2025-11-13	Warnings	Exact identifier ndc (product): 43406-0114 ndc11 (package): 43406011401

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.