Home FDA labels 2b9ed194-def5-363e-e063-6294a90a8cdc D-104 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-104
Generic name APIUM GRAVEOLENS WHOLE, ASCLEPIAS INCARNATA ROOT, CALCIUM ARSENATE, CAMPHOR (NATURAL), ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHRASIA STRICTA, FERROUS IODIDE, ICHTHAMMOL, SCABIES LESION LYSATE (HUMAN), THUJA OCCIDENTALIS LEAFY TWIG, AND TRIFOLIUM REPENS FLOWER
Manufacturer DNA Labs, Inc.
Product type HUMAN OTC DRUG
SPL set ID 09c3912a-71ba-4814-8b91-d0e787b542bf
SPL ID 2b9ed194-def5-363e-e063-6294a90a8cdc
Version 3
Effective date 2025-01-13
Source export date 2026-09-28
Source partition 7
Source file https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:45:18 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 · 20 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name D-104 openfda.brand_name generic name APIUM GRAVEOLENS WHOLE, ASCLEPIAS INCARNATA ROOT, CALCIUM ARSENATE, CAMPHOR (NATURAL), ECHINACEA ANGUSTIFOLIA, EUPATORIUM PERFOLIATUM FLOWERING TOP, EUPHRASIA STRICTA, FERROUS IODIDE, ICHTHAMMOL, SCABIES LESION LYSATE (HUMAN), THUJA OCCIDENTALIS LEAFY TWIG, AND TRIFOLIUM REPENS FLOWER openfda.generic_name manufacturer name DNA Labs, Inc. openfda.manufacturer_name ndc package 58264-0110-1 openfda.package_ndc ndc product 58264-0110 openfda.product_ndc ndc11 package 58264011001 derived:openfda.package_ndc spl id 2b9ed194-def5-363e-e063-6294a90a8cdc id spl set id 09c3912a-71ba-4814-8b91-d0e787b542bf set_id unii C9642I91WL openfda.unii unii 95OX15I8ZU openfda.unii unii 15V0BLB71G openfda.unii unii NQ14646378 openfda.unii unii 1NT28V9397 openfda.unii unii 49Y788T742 openfda.unii unii VB06AV5US8 openfda.unii unii N20HL7Q941 openfda.unii unii 5UAU16Z1U4 openfda.unii unii 1W0775VX6E openfda.unii unii 4N9UU1HQKG openfda.unii unii F5452U54PN 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.