Ambrosia artemisiaefolia

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
Ambrosia artemisiaefolia
Generic name
AMBROSIA ARTEMISIIFOLIA
Manufacturer
Boiron
Product type
HUMAN OTC DRUG
SPL set ID
8427717f-4d1a-54b5-e053-2a91aa0a3d00
SPL ID
10e04d03-329d-090f-e063-6294a90a6c72
Version
8
Effective date
2024-02-08
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:34:57
Harmonized routes table
Harmonized routes
ORAL

Reported adverse events (FAERS/openFDA)#

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