FDA.reportPublic FDA data

Bronchial Cough

Manufacturer
Hyland's Inc.
Effective date
2022-11-30
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 21:45:54

Label at a glance#

ProductBronchial Cough
Active ingredientPOTASSIUM DICHROMATE, RUMEX CRISPUS ROOT, SANGUINARIA CANADENSIS ROOT
Label structure9 sections

Indications and uses

Relief of symptoms of cough due to common cold, especially coughs with mucus production and a sensation of tickling in the throat.

Dosage and administration

Adults and children 12 years and over: dissolve 2-3 tablets under tongue every 4 hours or as needed. Children 6-12 years of age: 1/2 adult dose.

Label contents#

Full prescribing information#

OTC - PURPOSE SECTION

Natural Relief for Coughs with Mucus Due to Cold

Drug Facts

SPL UNCLASSIFIED SECTION

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Purpose

Kali Bichromicum 6X HPUS

cough, mucus discharge, tickling in throat

Rumex Crispus 6X HPUS

cough, mucus discharge

Sanguinaria Canadensis 6X HPUS

tickling cough, excessive mucus

“HPUS” indicates the active ingredients are in the official Homeopathic Pharmacopœia of the United States.

Uses

INDICATIONS & USAGE SECTION

Relief of symptoms of cough due to common cold, especially coughs with mucus production and a sensation of tickling in the throat.

WARNINGS SECTION

OTC - STOP USE SECTION

Stop use and ask a doctor if:  • symptoms persist for more than 7 days or worsen • cough persists for more than 7 days, tends to recur, or is accompanied by a rash, persistent headache, fever that lasts for more than three days or if new symptoms occur

Do not take this product

SPL UNCLASSIFIED SECTION

For persistent or chronic cough such as occurs with smoking, asthma or emphysema, or if cough is accompanied by excessive phlegm (mucus) unless directed by a doctor.

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental overdose, get medical help or contact a Poison Control Center immediately.

In case of emergency

SPL UNCLASSIFIED SECTION

In case of emergency, contact a medical professional or Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years and over: dissolve 2-3 tablets under tongue every 4 hours or as needed.

Children 6-12 years of age: 1/2 adult dose.

OTHER SAFETY INFORMATION

Other information • do not use if imprinted tamper band is broken or missing  • Hyland’s may be contacted for emergency

information about our products 24 hours a day, 7 days per week at (800) 624-9659

Inactive ingredients

INACTIVE INGREDIENT SECTION

Acacia Gum, Lactose N.F.

Questions or comments?

OTC - QUESTIONS SECTION

(800) 624-9659

PRINCIPAL DISPLAY PANEL-100 TABLET BOTTLE CARTON

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 54973-3222-1

Hyland's®

HOMEOPATHIC

Bronchial

Cough

Natural Relief for Coughs

with Mucus Due to Cold*

100

TABLETS

CartonCarton

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
54973-322254973-3222-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Name, UNII, Kind table
NameUNIIKind
ACACIA5C5403N26OIACT
LACTOSE MONOHYDRATEEWQ57Q8I5XIACT
POTASSIUM DICHROMATET4423S18FMACTIB
RUMEX CRISPUS ROOT9N1RM2S62CACTIB
SANGUINARIA CANADENSIS ROOTN9288CD508ACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
0812acaf-b409-9b85-e063-6294a90a39e75d0320c8-f764-7be4-e053-2a91aa0a14662023-10-19WarningsExact identifier
spl set id: 5d0320c8-f764-7be4-e053-2a91aa0a1466

Reported adverse events (FAERS/openFDA)#

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