Home FDA labels ff28cb48-6713-4c91-b05c-bbc92b795c1d ENT Support 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 ENT Support
Generic name PULSATILLA (PRATENSIS), EUPHORBIUM OFFICINARUM, LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, ARGENTUM NITRICUM, HEPAR SULPHURIS CALCAREUM, INFLUENZINUM (2022-2023), SINUSITISINUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, GALLICUM ACIDUM, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH)
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID be9efe32-f461-4d33-92ee-852069533176
SPL ID ff28cb48-6713-4c91-b05c-bbc92b795c1d
Version 2
Effective date 2024-01-15
Source export date 2026-09-28
Source partition 2
Source file https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256 cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run 20260929T050834Z
Imported at 2026-09-29 05:15:22 Harmonized routes table Harmonized routes ORAL
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 ENT Support openfda.brand_name generic name PULSATILLA (PRATENSIS), EUPHORBIUM OFFICINARUM, LUFFA OPERCULATA, MERCURIUS IODATUS RUBER, ARGENTUM NITRICUM, HEPAR SULPHURIS CALCAREUM, INFLUENZINUM (2022-2023), SINUSITISINUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, GALLICUM ACIDUM, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH) openfda.generic_name manufacturer name Deseret Biologicals, Inc. openfda.manufacturer_name ndc package 43742-2061-1 openfda.package_ndc ndc product 43742-2061 openfda.product_ndc ndc11 package 43742206101 derived:openfda.package_ndc spl id ff28cb48-6713-4c91-b05c-bbc92b795c1d id spl set id be9efe32-f461-4d33-92ee-852069533176 set_id unii 48339473OT openfda.unii unii 1TI1O9028K openfda.unii unii 95IT3W8JZE openfda.unii unii 4D7G21HDBC openfda.unii unii H2198F8ZNA openfda.unii unii 17RH99LQ7G openfda.unii unii B575563DM5 openfda.unii unii C4MO6809HU openfda.unii unii 8E272251DI openfda.unii unii 34C49NV47P openfda.unii unii 9IOA40ANG6 openfda.unii unii 514B9K0L10 openfda.unii unii TBV2PPG6EF openfda.unii unii R03O05RB0P openfda.unii unii 1MBW07J51Q openfda.unii unii P483J7GX6D 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: Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use. Tamper seal: "Sealed for Your Protection." Do not use if seal is broken or missing.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.