Lungs and Bronchial Relief

Product NDC
57955-9991
Type
HUMAN OTC DRUG
Nonproprietary name
Ammonium carbonicum, Antimonium arsenicicum, Antimonium tartaricum, Arsenicum album, Bromium, Carbo vegetabilis, Chlorinum, Kali carbonicum, Lobelia inflata, Stannum metallicum, Sulphuricum acidum.
Dosage form
LIQUID
Route
ORAL
Labeler
King Bio Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Substance
ACTIVATED CHARCOAL; AMMONIUM CARBONATE; ANTIMONY ARSENATE; ANTIMONY POTASSIUM TARTRATE; ARSENIC TRIOXIDE; BROMINE; CHLORINE; LOBELIA INFLATA WHOLE; POTASSIUM CARBONATE; SULFURIC ACID; TIN
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
57955-9991-259 mL in 1 BOTTLE, SPRAY (57955-9991-2) 2025-10-20NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Lungs and Bronchial ReliefKing Bio Inc.2026-03-02HUMAN OTC DRUG LABEL2