AB

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
AB
Generic name
ACONITUM NAPELLUS, BRYONIA CRETICA
Manufacturer
MARCO PHARMA INTERNATIONAL LLC
Product type
HUMAN OTC DRUG
SPL set ID
2d81c13f-102a-6741-e063-6294a90aee84
SPL ID
483ad8b7-56c6-1dc3-e063-6394a90abb23
Version
2
Effective date
2026-01-12
Source export date
2026-09-28
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:29:23
Harmonized routes table
Harmonized routes
ORAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

IF SYMPTOMS PERSIST MORE THAN A FEW DAYS, CONTACT LICENSED PRACTIONER.

Reported adverse events (FAERS/openFDA)#

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