BHI Mucus Tablet

Manufacturer: MediNatura Inc
Effective date: 2022-12-14
Label type: HUMAN OTC DRUG LABEL
Version: 7
Source: full-release
Hydrated at: 2026-06-01 02:18:53

Label at a glance#

ProductMucus Relief

Active ingredientANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE HEPATICA VAR. OBTUSA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, LOBARIA PULMONARIA

Label structure7 sections

Indications and uses

For the temporary relief of minor chest congestion and cough due to mucus build-up

Dosage and administration

At first sign of symptoms: Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage. Standard dosage: Adults and children 4 years and older : Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours. For children under 4, consult your health professional. Allow tablets to dissolve completely in the mouth, do not swallow.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Each tablet contains:

Antimonium tartaricum 5X, *Belladonna 6X, *Bryonia alba 6X, *Hepatica triloba 6X, *Hyoscyamus niger 5X, *Ipecacuanha 6X, *Lobelia inflata 4X, *Pertussinum 30X, *Sticta pulmonaria 5X 33.3 mg each.

*Natural Ingredients

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Dextrose, Magnesium Stearate, Maltodextrin

PURPOSE

OTC - PURPOSE SECTION

Mucus Relief Tablets

Relieves:

• Chest Congestion

• Mucus Build-up

• Cough

Uses:

INDICATIONS & USAGE SECTION

For the temporary relief of minor chest congestion and cough due to mucus build-up

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

At first sign of symptoms:

Adults and children 4 years and older: 1 tablet every 1/2 to 1 hour until symptoms lessen, then continue with standard dosage.

Standard dosage: Adults and children 4 years and older: Take 1-2 tablets every 4 to 6 hours. Do not exceed 12 tablets in 24 hours.

For children under 4, consult your health professional.

Allow tablets to dissolve completely in the mouth, do not swallow.

KEEP OUT OF REACH OF CHILDREN

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BHI Mucus Tablet

Add image transcription here...

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
ed912195-5da0-0f2f-6f4b-3ef17710cbe3	Product name	1	20140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
62795-1012-2	Mucus Relief	100 in 1 BOTTLE	TABLET	100	7
62795-1012-3	Mucus Relief	100 in 1 BOTTLE	TABLET	100	7
62795-1012-3	Mucus Relief	1 in 1 CARTON	TABLET	1	7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
62795-1012	MUCUS RELIEF (ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, AND LOBARIA PULMONARIA) TABLET [MEDINATURA INC]	7	Current NDC, Legacy NDC, 3 package rows	20221217_6338dc4f-b2d9-4b9a-a397-0440cbd1345a.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
62795-1012-2	EA - Each	62795-1012	89162f82-e659-49fc-8c8b-369415a09ad6	1	2015-10-02
62795-1012-3	EA - Each	62795-1012	64a4cabc-b936-4ae7-bb0b-099b98d7075e	1	2023-06-06

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ANEMONE AMERICANA	ACTIVE INGREDIENT	6ICN6T7FEM	1
ANTIMONY POTASSIUM TARTRATE	ACTIVE INGREDIENT	DL6OZ476V3	1
ATROPA BELLADONNA	ACTIVE INGREDIENT	WQZ3G9PF0H	1
BRYONIA ALBA WHOLE	ACTIVE INGREDIENT	56K0VVT47P	1
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED	ACTIVE INGREDIENT	U364V64HUN	1
HYOSCYAMUS NIGER	ACTIVE INGREDIENT	4WRK2153H3	1
IPECAC	ACTIVE INGREDIENT	62I3C8233L	1
LOBARIA PULMONARIA	ACTIVE INGREDIENT	D1YM0P5Z2T	1
LOBELIA INFLATA	ACTIVE INGREDIENT	9PP1T3TC5U	1
ANEMONE AMERICANA	ACTIVE MOIETY	6ICN6T7FEM	1
ANTIMONY CATION (3+)	ACTIVE MOIETY	069647RPT5	1
ATROPA BELLADONNA	ACTIVE MOIETY	WQZ3G9PF0H	1
BRYONIA ALBA WHOLE	ACTIVE MOIETY	56K0VVT47P	1
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED	ACTIVE MOIETY	U364V64HUN	1
HYOSCYAMUS NIGER	ACTIVE MOIETY	4WRK2153H3	1
IPECAC	ACTIVE MOIETY	62I3C8233L	1
LOBARIA PULMONARIA	ACTIVE MOIETY	D1YM0P5Z2T	1
LOBELIA INFLATA	ACTIVE MOIETY	9PP1T3TC5U	1
LACTOSE	INACTIVE INGREDIENT	J2B2A4N98G	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	1

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

Mucus Relief
ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, and LOBARIA PULMONARIA
ANTIMONY POTASSIUM TARTRATE
ANTIMONY CATION (3+)
ATROPA BELLADONNA
BRYONIA ALBA WHOLE
ANEMONE HEPATICA VAR. OBTUSA
HYOSCYAMUS NIGER
IPECAC
LOBELIA INFLATA
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED
LOBARIA PULMONARIA
MAGNESIUM STEARATE
MALTODEXTRIN
DEXTROSE

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
62795-1012	62795-1012-3, 62795-1012-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ANTIMONY POTASSIUM TARTRATE	DL6OZ476V3	ACTIB
ATROPA BELLADONNA	WQZ3G9PF0H	ACTIB
BRYONIA ALBA WHOLE	56K0VVT47P	ACTIB
ANEMONE HEPATICA VAR. OBTUSA	6ICN6T7FEM	ACTIB
HYOSCYAMUS NIGER	4WRK2153H3	ACTIB
IPECAC	62I3C8233L	ACTIB
LOBELIA INFLATA	9PP1T3TC5U	ACTIB
HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED	U364V64HUN	ACTIB
LOBARIA PULMONARIA	D1YM0P5Z2T	ACTIB
MAGNESIUM STEARATE	70097M6I30	IACT
MALTODEXTRIN	7CVR7L4A2D	IACT
DEXTROSE	IY9XDZ35W2	IACT

Source Document#

Source XML

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 6 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
LACTOSE	LACTOSE	J2B2A4N98G	TABLET / ORAL	2500 mg		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
LACTOSE	LACTOSE	J2B2A4N98G	TABLET / ORAL	2500 mg		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
LACTOSE	LACTOSE	J2B2A4N98G	TABLET / ORAL	2500 mg		Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
MAGNESIUM STEARATE	MAGNESIUM STEARATE	70097M6I30	TABLET / ORAL		980 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
MAGNESIUM STEARATE	MAGNESIUM STEARATE	70097M6I30	TABLET / ORAL		980 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
MAGNESIUM STEARATE	MAGNESIUM STEARATE	70097M6I30	TABLET / ORAL		980 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Mucus Relief	ANTIMONY POTASSIUM TARTRATE, ATROPA BELLADONNA, BRYONIA ALBA WHOLE, ANEMONE AMERICANA, HYOSCYAMUS NIGER, IPECAC, LOBELIA INFLATA, HUMAN SPUTUM, BORDETELLA PERTUSSIS INFECTED, AND LOBARIA PULMONARIA	MediNatura Inc	6338dc4f-b2d9-4b9a-a397-0440cbd1345a	2022-12-14	Warnings	Exact identifier ndc (package): 62795-1012-2 ndc (package): 62795-1012-3 ndc (product): 62795-1012 ndc11 (package): 62795101203 ndc11 (package): 62795101202 spl id: 906bf8a5-cca6-4a15-9de3-4f4111da1c2f spl set id: 6338dc4f-b2d9-4b9a-a397-0440cbd1345a

Reported adverse events (FAERS/openFDA)#

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