Home FDA labels 0e76db01-1825-6a4e-e063-6294a90a6e32 D09 SNS-DRN 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 D09 SNS-DRN
Generic name AMBROSIA ARTEMISIAEFOLIA, ARALIA RACEMOSA, ARNICA MONTANA, CALENDULA OFFICINALIS, CHROMICUM ACIDUM, ECHINACEA PURPUREA, EUCALYPTOL, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC VACCINUM, MERCURIUS IODATUS FLAVUS, MERCURIUS SULPHURATUS RUBER, NATRUM ARSENICICUM, ROSA DAMASCENA, SABADILLA, SANGUINARINUM NITRICUM, SYMPHYTUM OFFICINALE
Manufacturer Apex Energetics Inc.
Product type HUMAN OTC DRUG
SPL set ID bc7efab4-7791-9759-e053-2a95a90a3109
SPL ID 0e76db01-1825-6a4e-e063-6294a90a6e32
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 05:19:35 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name D09 SNS-DRN openfda.brand_name generic name AMBROSIA ARTEMISIAEFOLIA, ARALIA RACEMOSA, ARNICA MONTANA, CALENDULA OFFICINALIS, CHROMICUM ACIDUM, ECHINACEA PURPUREA, EUCALYPTOL, KALI BICHROMICUM, KALI MURIATICUM, KALI SULPHURICUM, LAC VACCINUM, MERCURIUS IODATUS FLAVUS, MERCURIUS SULPHURATUS RUBER, NATRUM ARSENICICUM, ROSA DAMASCENA, SABADILLA, SANGUINARINUM NITRICUM, SYMPHYTUM OFFICINALE openfda.generic_name manufacturer name Apex Energetics Inc. openfda.manufacturer_name ndc package 63479-0409-1 openfda.package_ndc ndc product 63479-0409 openfda.product_ndc ndc11 package 63479040901 derived:openfda.package_ndc spl id 0e76db01-1825-6a4e-e063-6294a90a6e32 id spl set id bc7efab4-7791-9759-e053-2a95a90a3109 set_id unii 917J3173FT openfda.unii unii O80TY208ZW openfda.unii unii T90W4582DU openfda.unii unii 21W82Q764G openfda.unii unii 18E7415PXQ openfda.unii unii HT0935F2JR openfda.unii unii 8LV49809UC openfda.unii unii M9VVZ08EKQ openfda.unii unii 1K573LC5TV openfda.unii unii 9W34L2CQ9A openfda.unii unii 660YQ98I10 openfda.unii unii 6NAF1689IO openfda.unii unii BOP122S791 openfda.unii unii QI7G114Y98 openfda.unii unii T4423S18FM openfda.unii unii RV6J6604TK openfda.unii unii ZI0T668SF1 openfda.unii unii 90ZQ7G407W 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 sinus discomfort, nasal discharge, sneezing, cough, 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.