Home FDA labels fd47b576-5f8b-4032-8795-968f13d6615b 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 (2021-2022), SINUSITISINUM, ASPERGILLUS NIGER, CANDIDA ALBICANS, GALLICUM ACIDUM, MUCOR RACEMOSUS, MUTABILE BACILLUS (BACH)
Manufacturer Deseret Biologicals, Inc.
Product type HUMAN OTC DRUG
SPL set ID 57067c80-d442-463a-babf-c5d3057cd9b4
SPL ID fd47b576-5f8b-4032-8795-968f13d6615b
Version 2
Effective date 2022-12-05
Source export date 2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 01:39:34 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 (2021-2022), 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 43742-2041-1 openfda.package_ndc ndc product 43742-2041 openfda.product_ndc ndc11 package 43742204101 derived:openfda.package_ndc spl id fd47b576-5f8b-4032-8795-968f13d6615b id spl set id 57067c80-d442-463a-babf-c5d3057cd9b4 set_id unii V529EJB2CX openfda.unii unii 48339473OT openfda.unii unii 1TI1O9028K openfda.unii unii VEH9U90EHX openfda.unii unii 95IT3W8JZE openfda.unii unii B93BQX9789 openfda.unii unii 4D7G21HDBC openfda.unii unii 17RH99LQ7G openfda.unii unii B575563DM5 openfda.unii unii C4MO6809HU openfda.unii unii 8E272251DI openfda.unii unii 9IOA40ANG6 openfda.unii unii 514B9K0L10 openfda.unii unii R03O05RB0P openfda.unii unii WD5E5VYM2E openfda.unii unii 1MBW07J51Q 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.