warnings
Warnings: Do not use if tamper evident cap is broken. If you are pregnant or nursing a baby, consult your doctor before using this product. If condition persists, recurs or worsens, discontinue use and consult your physician.
EZ-Detox Super Drainage Formula
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
- Brand name
- EZ-Detox Super Drainage Formula
- Generic name
- AESCULUS HIPPOCASTANUM BARK,ANTIMONY TRISULFIDE,SILVER NITRATE,ARNICA MONTANA,BERBERIS VULGARIS WHOLE,ACTIVATED CHARCOAL,CEANOTHUS AMERICANUS WHOLE,CHOLESTEROL,CINCHONA BARK,CYNARA SCOLYMUS LEAF,EQUISETUM ARVENSE TOP,CONYZA CANADENSIS,FUCUS VESICULOSUS,GINKGO,HAMAMELIS VIRGINIANA LEAF,CHAMAELIRIUM LUTEUM ROOT,GOLDENSEAL,ARCTIUM LAPPA ROOT,LESPEDEZA CAPITATA FLOWERING TOP,RANUNCULUS BULBOSUS,DAIKON,ROBINIA PSEUDOACACIA BARK,TARAXACUM PALUSTRE ROOT,VIBURNUM PRUNIFOLIUM BARK,VITIS VINIFERA WHOLE
- Manufacturer
- Homeocare Laboratories
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5a07e95d-08a8-4a54-bd04-3679a7b856c8
- SPL ID
- 7e58351d-e93f-bd9c-e053-2991aa0ab3d0
- Version
- 2
- Effective date
- 2018-12-31
- Source export date
- 2026-09-28
- Source partition
- 6
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:37:12
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.