FDA label 252d7be1-68c6-4139-8a1a-98cc7fd9aa4e

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)

SPL set ID: c0c9aaff-c8ae-4121-9869-e0e90f5f0ae9
SPL ID: 252d7be1-68c6-4139-8a1a-98cc7fd9aa4e
Version: 32749
Effective date: 2021-10-19
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 06:34:35

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		252d7be1-68c6-4139-8a1a-98cc7fd9aa4e	id
spl set id		c0c9aaff-c8ae-4121-9869-e0e90f5f0ae9	set_id

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

Warning This product is forbidden for patients with heart bypass or stents. This product is forbidden for critically ill patients and cancer patients. This product is forbidden for parturient women. This product is forbidden for patients with internal or external bleeding and subcutaneous hemorrhage. This product is forbidden for severe diabetic patients (severe skin ulceration), cardiovascular and cerebrovascular patients, severely hypertensive patients. For women who are allergic to Chinese herbal medicine during menstruation, use it with caution. This product is only for foot bathing and foot health care. External use only.

Reported adverse events (FAERS/openFDA)#

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