bronchial cough therapy
Generic: antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted -
Labeler: trp companyDrug Facts
Product Profile
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 -
Labeler
trp company
Dosage Form
TABLET, ORALLY DISINTEGRATING
Routes
Active Ingredients
antimony potassium tartrate 6 [hp_C]/1, calcium sulfide 6 [hp_C]/1, drosera rotundifolia 6 [hp_C]/1, echinacea, unspecified 6 [hp_C]/1, human sputum, bordetella pertussis infected 18 [hp_C]/1, protortonia cacti 6 [hp_C]/1, spongia officinalis skeleton, roasted 6 [hp_C]/1
Manufacturer
Identifiers & Regulatory
Product NDC
17312-018
Product ID
17312-018_4604e0a2-5b75-5e33-e063-6294a90a6601
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2011-12-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
17312018
Hyphenated Format
17312-018
Supplemental Identifiers
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
bronchial cough therapy (source: ndc)
Generic Name
antimony potassium tartrate - protortonia cacti - drosera rotundifolia - echinacea, unspecified - calcium sulfide - human sputum, bordetella pertussis infected - spongia officinalis skeleton, roasted - (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 6 [hp_C]/1
- 18 [hp_C]/1
Packaging
- 1 BOTTLE in 1 PACKAGE (17312-018-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE
Packages (1)
Ingredients (7)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4604e0a2-5b75-5e33-e063-6294a90a6601", "openfda": {"upc": ["0858961001181"], "unii": ["DL6OZ476V3", "1MBW07J51Q", "QR44N9XPJQ", "4N9P6CC1DX", "U364V64HUN", "LZB7TFX1LT", "1PIP394IID"], "spl_set_id": ["f87ad18c-689b-4279-8098-a075ce62bff7"], "manufacturer_name": ["TRP Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 PACKAGE (17312-018-14) / 70 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE", "package_ndc": "17312-018-14", "marketing_start_date": "20111201"}], "brand_name": "Bronchial Cough Therapy", "product_id": "17312-018_4604e0a2-5b75-5e33-e063-6294a90a6601", "dosage_form": "TABLET, ORALLY DISINTEGRATING", "product_ndc": "17312-018", "generic_name": "ANTIMONY POTASSIUM TARTRATE - PROTORTONIA CACTI - DROSERA ROTUNDIFOLIA - ECHINACEA, UNSPECIFIED - CALCIUM SULFIDE - HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED - SPONGIA OFFICINALIS SKELETON, ROASTED -", "labeler_name": "TRP Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bronchial Cough Therapy", "active_ingredients": [{"name": "ANTIMONY POTASSIUM TARTRATE", "strength": "6 [hp_C]/1"}, {"name": "CALCIUM SULFIDE", "strength": "6 [hp_C]/1"}, {"name": "DROSERA ROTUNDIFOLIA", "strength": "6 [hp_C]/1"}, {"name": "ECHINACEA, UNSPECIFIED", "strength": "6 [hp_C]/1"}, {"name": "HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED", "strength": "18 [hp_C]/1"}, {"name": "PROTORTONIA CACTI", "strength": "6 [hp_C]/1"}, {"name": "SPONGIA OFFICINALIS SKELETON, ROASTED", "strength": "6 [hp_C]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20111201", "listing_expiration_date": "20261231"}