Home FDA labels 0e76df45-c9e7-7085-e063-6294a90a6423 D02 DIGESTIVE DRAINAGE 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 D02 DIGESTIVE DRAINAGE
Generic name ALOE, ACTIVATED CHARCOAL, COLCHICUM AUTUMNALE BULB, COLLINSONIA CANADENSIS ROOT, CUCURBITA PEPO FLOWER, DRYOPTERIS FILIX-MAS ROOT, INDOLE, SKIM MILK, LYCOPODIUM CLAVATUM SPORE, ACHILLEA MILLEFOLIUM, SODIUM SULFATE, FRANGULA PURSHIANA BARK, SCROPHULARIA NODOSA, SKATOLE, TARAXACUM OFFICINALE, TARTARIC ACID
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID ba8734bf-920c-0ce4-e053-2a95a90a0705
SPL ID 0e76df45-c9e7-7085-e063-6294a90a6423
Version 2
Effective date 2024-01-08
Source export date 2026-09-28
Source partition 3
Source file https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:19:33 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 · 24 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name D02 DIGESTIVE DRAINAGE openfda.brand_name generic name ALOE, ACTIVATED CHARCOAL, COLCHICUM AUTUMNALE BULB, COLLINSONIA CANADENSIS ROOT, CUCURBITA PEPO FLOWER, DRYOPTERIS FILIX-MAS ROOT, INDOLE, SKIM MILK, LYCOPODIUM CLAVATUM SPORE, ACHILLEA MILLEFOLIUM, SODIUM SULFATE, FRANGULA PURSHIANA BARK, SCROPHULARIA NODOSA, SKATOLE, TARAXACUM OFFICINALE, TARTARIC ACID openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0402-1 openfda.package_ndc ndc product 63479-0402 openfda.product_ndc ndc11 package 63479040201 derived:openfda.package_ndc spl id 0e76df45-c9e7-7085-e063-6294a90a6423 id spl set id ba8734bf-920c-0ce4-e053-2a95a90a0705 set_id unii 2P3VWU3H10 openfda.unii unii 2FXJ6SW4PK openfda.unii unii 993QHL78E6 openfda.unii unii 6A001Y4M5A openfda.unii unii 8724FJW4M5 openfda.unii unii 0YPR65R21J openfda.unii unii 4VBP01X99F openfda.unii unii O2630F3XDR openfda.unii unii 39981FM375 openfda.unii unii 413MGP37HQ openfda.unii unii W4888I119H openfda.unii unii 9W945B5H7R openfda.unii unii V5VD430YW9 openfda.unii unii C0ZK0RRF5X openfda.unii unii C88X29Y479 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: If pregnant or breastfeeding , ask a health professional before use. Do not use if clear seal over the cap is broken or missing. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if indigestion, bloating, fatigue, difficult bowel movements, flatulence, diarrhea, or other symptoms do not improve within 7 days or are accompanied by fever.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.