Home FDA labels 2b9ea85a-2109-8fa9-e063-6294a90a9ef1 D-30 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 D-30
Generic name STRONTIUM SALICYLATE, METHENAMINE, COLCHICUM AUTUMNALE BULB, BLACK COHOSH, ARNICA MONTANA, CALENDULA OFFICINALIS FLOWERING TOP, SOLANUM DULCAMARA WHOLE, HYPERICUM PERFORATUM, STRYCHNOS NUX-VOMICA SEED, ATROPA BELLADONNA, ECHINACEA ANGUSTIFOLIA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ACHILLEA MILLEFOLIUM, AND TOXICODENDRON PUBESCENS LEAF
Manufacturer DNA Labs, Inc.
Product type HUMAN OTC DRUG
SPL set ID 0e74e654-4bda-4969-89be-8ab89014bce2
SPL ID 2b9ea85a-2109-8fa9-e063-6294a90a9ef1
Version 3
Effective date 2025-01-13
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 05:56:47 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 · 22 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name D-30 openfda.brand_name generic name STRONTIUM SALICYLATE, METHENAMINE, COLCHICUM AUTUMNALE BULB, BLACK COHOSH, ARNICA MONTANA, CALENDULA OFFICINALIS FLOWERING TOP, SOLANUM DULCAMARA WHOLE, HYPERICUM PERFORATUM, STRYCHNOS NUX-VOMICA SEED, ATROPA BELLADONNA, ECHINACEA ANGUSTIFOLIA, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, ACHILLEA MILLEFOLIUM, AND TOXICODENDRON PUBESCENS LEAF openfda.generic_name manufacturer name DNA Labs, Inc. openfda.manufacturer_name ndc package 58264-0030-1 openfda.package_ndc ndc product 58264-0030 openfda.product_ndc ndc11 package 58264003001 derived:openfda.package_ndc spl id 2b9ea85a-2109-8fa9-e063-6294a90a9ef1 id spl set id 0e74e654-4bda-4969-89be-8ab89014bce2 set_id unii 2FXJ6SW4PK openfda.unii unii XK4IUX8MNB openfda.unii unii 269XH13919 openfda.unii unii 993QHL78E6 openfda.unii unii O80TY208ZW openfda.unii unii G72JA9DHK5 openfda.unii unii 18E7415PXQ openfda.unii unii 6IO182RP7A openfda.unii unii VB06AV5US8 openfda.unii unii OGF9EV99TC openfda.unii unii WQZ3G9PF0H openfda.unii unii J50OIX95QV openfda.unii unii K73E24S6X9 openfda.unii unii T7S323PKJS 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. If pregnant or breastfeeding, ask a healthcare professional before use. 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.