Home FDA labels e847b14d-de88-4d5d-8fba-c528919bbfc8 Breathe 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 Breathe
Generic name ARGENTUM NITRICUM, NATRUM MURIATICUM, SULPHUR, ACONITUM NAPELLUS, ARSENICUM ALBUM, RHUS TOX, ADENOSINUM CYCLOPHOSPHORICUM, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, LUNG (SUIS), MUCOSA NASALIS SUIS, PANTOTHENIC ACID, SARCOLACTICUM ACIDUM, ACETYLCHOLINE CHLORIDE, COUMARINUM, MALVIN, DYSENTERY BACILLUS, PROTEUS (MORGANI)
Manufacturer Deseret Biologicals, Inc
Product type HUMAN OTC DRUG
SPL set ID 8dbdd623-a486-4cf8-acdb-ad051dc74348
SPL ID e847b14d-de88-4d5d-8fba-c528919bbfc8
Version 2
Effective date 2024-03-15
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 05:15:23 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 · 26 matching rows.
Type, Scope, Identifier table Type Scope Identifier Source field brand name Breathe openfda.brand_name generic name ARGENTUM NITRICUM, NATRUM MURIATICUM, SULPHUR, ACONITUM NAPELLUS, ARSENICUM ALBUM, RHUS TOX, ADENOSINUM CYCLOPHOSPHORICUM, FUNICULUS UMBILICALIS SUIS, GLANDULA SUPRARENALIS SUIS, LUNG (SUIS), MUCOSA NASALIS SUIS, PANTOTHENIC ACID, SARCOLACTICUM ACIDUM, ACETYLCHOLINE CHLORIDE, COUMARINUM, MALVIN, DYSENTERY BACILLUS, PROTEUS (MORGANI) openfda.generic_name manufacturer name Deseret Biologicals, Inc openfda.manufacturer_name ndc package 43742-1263-1 openfda.package_ndc ndc product 43742-1263 openfda.product_ndc ndc11 package 43742126301 derived:openfda.package_ndc spl id e847b14d-de88-4d5d-8fba-c528919bbfc8 id spl set id 8dbdd623-a486-4cf8-acdb-ad051dc74348 set_id unii 7GL3G1COB3 openfda.unii unii I9I120531L openfda.unii unii 19F5HK2737 openfda.unii unii 1EP6R5562J openfda.unii unii ID3Z1X61WY openfda.unii unii F9S9FFU82N openfda.unii unii 95IT3W8JZE openfda.unii unii 451W47IQ8X openfda.unii unii 6IO182RP7A openfda.unii unii S7V92P67HO openfda.unii unii AF73293C2R openfda.unii unii 56X6LID5ZY openfda.unii unii A4VZ22K1WT openfda.unii unii 398IYQ16YV openfda.unii unii 70FD1KFU70 openfda.unii unii E0399OZS9N openfda.unii unii U0NQ8555JD openfda.unii unii 118OYG6W3H 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 breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, contact a physician or Poison Control Center right away. Tamper Evident: 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.