Bronchial Cough Therapy

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: Bronchial Cough Therapy
Generic name: ANTIMONY POTASSIUM TARTRATE - PROTORTONIA CACTI - DROSERA ROTUNDIFOLIA - ECHINACEA, UNSPECIFIED - CALCIUM SULFIDE - HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - SPONGIA OFFICINALIS SKELETON, ROASTED -
Manufacturer: TRP Company
Product type: HUMAN OTC DRUG
SPL set ID: f87ad18c-689b-4279-8098-a075ce62bff7
SPL ID: 4604e0a2-5b75-5e33-e063-6294a90a6601
Version: 8
Effective date: 2025-12-15
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 05:19:34

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Bronchial Cough Therapy	openfda.brand_name
generic name		ANTIMONY POTASSIUM TARTRATE - PROTORTONIA CACTI - DROSERA ROTUNDIFOLIA - ECHINACEA, UNSPECIFIED - CALCIUM SULFIDE - HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - SPONGIA OFFICINALIS SKELETON, ROASTED -	openfda.generic_name
manufacturer name		TRP Company	openfda.manufacturer_name
ndc	package	17312-018-14	openfda.package_ndc
ndc	product	17312-018	openfda.product_ndc
ndc11	package	17312001814	derived:openfda.package_ndc
spl id		4604e0a2-5b75-5e33-e063-6294a90a6601	id
spl set id		f87ad18c-689b-4279-8098-a075ce62bff7	set_id
unii		QR44N9XPJQ	openfda.unii
unii		LZB7TFX1LT	openfda.unii
unii		U364V64HUN	openfda.unii
unii		DL6OZ476V3	openfda.unii
unii		4N9P6CC1DX	openfda.unii
unii		1PIP394IID	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 USE ONLY AFTER DIAGNOSIS BY A PHYSICIAN. This product is a not a fast acting (rescue) inhaler. This product is intended to complement, not replace, standard medical treatment. Initial worsening of symptoms may occur. A physician should always be consulted to rule out serious causes. In case of overdose, get medical help or contact a Poison Control Center right away. Stop use and ask a doctor if: You experience worsening symptoms. If symptoms last longer than 7 days.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.