Home FDA labels 2b9edb0e-499a-f422-e063-6294a90ae8fa D-88 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-88
Generic name COCCULUS INDICUS, NATRUM MURIATICUM, HELONIAS DIOICA, CALCAREA PHOSPHORICUM, IGNATIA AMARA, MAGNESIA PHOSPHORICUM, CIMICIFUGA RACEMOSA, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS, SEPIA, KALIUM PHOSPHORICUM, ZINCUM METALLICUM, PITUITARY, ADRENAL, OVARIAN
Manufacturer DNA Labs, Inc.
Product type HUMAN OTC DRUG
SPL set ID 1eefff9c-d86c-44ef-b968-9a8c5a9c5403
SPL ID 2b9edb0e-499a-f422-e063-6294a90ae8fa
Version 3
Effective date 2025-01-13
Source export date 2026-09-28
Source partition 4
Source file https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:26:31 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 D-88 openfda.brand_name generic name COCCULUS INDICUS, NATRUM MURIATICUM, HELONIAS DIOICA, CALCAREA PHOSPHORICUM, IGNATIA AMARA, MAGNESIA PHOSPHORICUM, CIMICIFUGA RACEMOSA, PASSIFLORA INCARNATA, VALERIANA OFFICINALIS, SEPIA, KALIUM PHOSPHORICUM, ZINCUM METALLICUM, PITUITARY, ADRENAL, OVARIAN openfda.generic_name manufacturer name DNA Labs, Inc. openfda.manufacturer_name ndc package 58264-0094-1 openfda.package_ndc ndc product 58264-0094 openfda.product_ndc ndc11 package 58264009401 derived:openfda.package_ndc spl id 2b9edb0e-499a-f422-e063-6294a90ae8fa id spl set id 1eefff9c-d86c-44ef-b968-9a8c5a9c5403 set_id unii CI71S98N1Z openfda.unii unii QDL83WN8C2 openfda.unii unii 7JM57I419K openfda.unii unii 66LZN1C747 openfda.unii unii 91D9GV0Z28 openfda.unii unii HF539G9L3Q openfda.unii unii 451W47IQ8X openfda.unii unii 1NM3M2487K openfda.unii unii M2776SWB29 openfda.unii unii JWF5YAW3QW openfda.unii unii 810258W28U openfda.unii unii CLF5YFS11O openfda.unii unii DQV54Y5H3U openfda.unii unii J41CSQ7QDS openfda.unii unii K73E24S6X9 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.