BAENOSIN

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
BAENOSIN
Generic name
PLATYCODON ROOT, LICORICE, JUJUBE, PEONY ROOT
Manufacturer
Lydia Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
874f9b81-80eb-05fd-e053-2a95a90afdeb
SPL ID
0ca8ac22-aaab-9d25-e063-6294a90a4541
Version
2
Effective date
2023-12-16
Source export date
2026-10-27
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run
20261027T193451Z
Imported at
2026-10-27 19:59:28
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

do not take this medicine if you have following symptoms symptoms of headaches, chills, and fever other than local symptoms such as spasm (red with blood), swelling, and pain at the same time

Reported adverse events (FAERS/openFDA)#

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