Home FDA labels 2b9edb0e-499f-f422-e063-6294a90ae8fa D134 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 D134
Generic name BLACK COHOSH, BRYONIA ALBA WHOLE, TOXICODENDRON PUBESCENS WHOLE, ARNICA MONTANA, CAUSTICUM, FERROSOFERRIC PHOSPHATE, SODIUM SULFATE ANHYDROUS, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM WHOLE, CITRULLUS COLOCYNTHIS WHOLE, SOLANUM DULCAMARA WHOLE, KALMIA LATIFOLIA WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, ARSENIC TRIOXIDE, AND TRIBASIC CALCIUM PHOSPHATE
Manufacturer DNA Labs, Inc.
Product type HUMAN OTC DRUG
SPL set ID a1d4d74a-75ca-45f8-8787-7ac6aa726932
SPL ID 2b9edb0e-499f-f422-e063-6294a90ae8fa
Version 3
Effective date 2025-01-13
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 05:37:00 Harmonized routes table Harmonized routes SUBLINGUAL
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 D134 openfda.brand_name generic name BLACK COHOSH, BRYONIA ALBA WHOLE, TOXICODENDRON PUBESCENS WHOLE, ARNICA MONTANA, CAUSTICUM, FERROSOFERRIC PHOSPHATE, SODIUM SULFATE ANHYDROUS, STRYCHNOS NUX-VOMICA SEED, RHODODENDRON AUREUM WHOLE, CITRULLUS COLOCYNTHIS WHOLE, SOLANUM DULCAMARA WHOLE, KALMIA LATIFOLIA WHOLE, MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE, ARSENIC TRIOXIDE, AND TRIBASIC CALCIUM PHOSPHATE openfda.generic_name manufacturer name DNA Labs, Inc. openfda.manufacturer_name ndc package 58264-0140-1 openfda.package_ndc ndc product 58264-0140 openfda.product_ndc ndc11 package 58264014001 derived:openfda.package_ndc spl id 2b9edb0e-499f-f422-e063-6294a90ae8fa id spl set id a1d4d74a-75ca-45f8-8787-7ac6aa726932 set_id unii 269XH13919 openfda.unii unii MM2Y21LFIT openfda.unii unii DD5FO1WKFU openfda.unii unii O80TY208ZW openfda.unii unii G72JA9DHK5 openfda.unii unii C1S185Y74S openfda.unii unii 91D9GV0Z28 openfda.unii unii HF539G9L3Q openfda.unii unii P1SWF7DK1Y openfda.unii unii 91GQH8I5F7 openfda.unii unii S7V92P67HO openfda.unii unii 56K0VVT47P openfda.unii unii Z70W98921V openfda.unii unii K73E24S6X9 openfda.unii unii 36KCS0R750 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 Use only if cap seal is unbroken. As with drugs if you are pregnant or nursing a baby seek professional advice before using this product. Keep this and all medication out of the reach of children.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.