CHEONGWIDAN-F

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
CHEONGWIDAN-F
Generic name
DRY GINGER, CINNAMON BARK, MENTHA HERB
Manufacturer
Lydia Co., Ltd.
Product type
HUMAN OTC DRUG
SPL set ID
2e1402a0-c818-5c7a-e063-6294a90a6b52
SPL ID
2e14020d-6d9a-579e-e063-6394a90aa5a0
Version
1
Effective date
2025-02-13
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:55:54
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

When using this product ■Do not use infants and toddlers under the age of seven. ■Do not use it for more than 1 month unless the symptoms improve. ■Do not change it to another container to prevent misuse and preserve quality. ■To keep the prescribed usage and capacity. Ask a doctor before use if you take other medication. If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children, In case of overdose, get medical help or contact a poison control center right away

Reported adverse events (FAERS/openFDA)#

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