Home FDA labels 58c8b270-59a9-1bba-e063-6394a90a3ed5 Drainage-Tone 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 Drainage-Tone
Generic name CALCAREA IODATA, CAPSICUM ANNUUM, COENZYME A, ECHINACEA ANGUSTIFOLIA, EQUISETUM ARVENSE, HYDRASTIS CANADENSIS, NADIDUM, NITRICUM ACIDUM, OLEUM MORRHUAE, PETROSELINUM SATIVUM, PHYTOLACCA DECANDRA, SCROPHULARIA NODOSA, SILICEA, SINAPIS ALBA, THUJA OCCIDENTALIS.
Manufacturer Energetix Corporation
Product type HUMAN OTC DRUG
SPL set ID 296b455e-27c5-4f6e-929d-c4ee75b7fb0e
SPL ID 58c8b270-59a9-1bba-e063-6394a90a3ed5
Version 12
Effective date 2026-08-11
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 05:56:39 Harmonized routes table 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.
Harmonized identifiers page 1 of 1 · 23 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Drainage-Tone openfda.brand_name generic name CALCAREA IODATA, CAPSICUM ANNUUM, COENZYME A, ECHINACEA ANGUSTIFOLIA, EQUISETUM ARVENSE, HYDRASTIS CANADENSIS, NADIDUM, NITRICUM ACIDUM, OLEUM MORRHUAE, PETROSELINUM SATIVUM, PHYTOLACCA DECANDRA, SCROPHULARIA NODOSA, SILICEA, SINAPIS ALBA, THUJA OCCIDENTALIS. openfda.generic_name manufacturer name Energetix Corporation openfda.manufacturer_name ndc package 64578-0142-1 openfda.package_ndc ndc product 64578-0142 openfda.product_ndc ndc11 package 64578014201 derived:openfda.package_ndc spl id 58c8b270-59a9-1bba-e063-6394a90a3ed5 id spl set id 296b455e-27c5-4f6e-929d-c4ee75b7fb0e set_id unii 00UK7646FG openfda.unii unii 11E6VI8VEG openfda.unii unii 25VR943RPP openfda.unii unii 411VRN1TV4 openfda.unii unii SAA04E81UX openfda.unii unii 1NT28V9397 openfda.unii unii ETJ7Z6XBU4 openfda.unii unii VB06AV5US8 openfda.unii unii 0U46U6E8UK openfda.unii unii ZW3Z11D0JV openfda.unii unii 1WZA4Y92EX openfda.unii unii BBL281NWFG openfda.unii unii 8EKI9QEE2H openfda.unii unii 1DP6Y6B65Z openfda.unii unii 7H443NUB2T openfda.unii
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 Warnings In case of overdose, get medical help or contact a Poison Control Center right away. If pregnant or breast feeding, ask a health professional before use. • Keep out of reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.