FDA.reportPublic FDA data

BMNP BM13 LIQUID

Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro | BM Private Limited
Effective date
2026-06-12
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-06-17 05:10:07

Label at a glance#

ProductBM BM13 DROPS
Active ingredientATROPA BELLADONNA, CUPRIC ACETATE, DROSERA ROTUNDIFOLIA WHOLE, NAPHTHALENE, LOBELIA INFLATA WHOLE, IPECAC, GRINDELIA HIRSUTULA FLOWERING TOP, ERIODICTYON CALIFORNICUM LEAF
Label structure9 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Belladonna 4X, Cupr acet 6X, Drosera 3X, Grindelia 4X, Ipecac 5X, Lob infl 2X, Naphth 12X, Yerba Santa 4X

INDICATIONS & USAGE SECTION

Uses*

Helps temporarily relieve: cough and throat irritation; and respiratory discomfort with mucus or congestion.

OTC - PURPOSE SECTION

Belladonna 4X (HPUS)......sudden cough, throat irritation
Cupr acet 6X (HPUS)......coughing fits, chest discomfort
Drosera 3X (HPUS)......dry cough, night cough, throat irritation
Grindelia 4X (HPUS)......bronchial discomfort, mucus accumulation
Ipecac 5X (HPUS)......nausea, coughing, throat irritation
Lob infl 2X (HPUS)......breathing discomfort, wheezing
Naphthalinum 12X (HPUS)......recurring cough, airway sensitivity
Yerba sant 4X (HPUS)......mucus, irritation

"HPUS" is the Homeopathic Pharmacopoeia of the United States.

DOSAGE & ADMINISTRATION SECTION

Use as directed.
Mix with half a cup of water and drink immediately. Repeat this process 3-4 times daily. Ages 12 and older: 10 drops. Ages 3 to 11: 5 drops. Ages under 3: consult your doctor.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

WARNINGS SECTION

Keep out of reach of children.

If pregnant or breastfeeding, ask a health professional before use.

Stop use and ask a doctor if symptoms persist or worsen.

If you have severe symptoms, consult a doctor before use.

INACTIVE INGREDIENT SECTION

Alcohol

HEALTH CLAIM SECTION

*Claims based on Traditional Homeopathic Practice, Not Accepted Medical Evidence, Not FDA Evaluated.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

BM13BM13

BM13BM13

BM13BM13

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-231382969-2313-1
85816-2013

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 9 matching rows.

Name, UNII, Kind table
NameUNIIKind
ALCOHOL3K9958V90MIACT
ATROPA BELLADONNAWQZ3G9PF0HACTIB
CUPRIC ACETATE39M11XPH03ACTIB
DROSERA ROTUNDIFOLIA WHOLEQR44N9XPJQACTIB
NAPHTHALENE2166IN72UNACTIB
LOBELIA INFLATA WHOLE9PP1T3TC5UACTIB
IPECAC62I3C8233LACTIB
GRINDELIA HIRSUTULA FLOWERING TOPIDB0NAZ6AIACTIB
ERIODICTYON CALIFORNICUM LEAF2Y7TIQ135HACTIB

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
BM BM13 DROPSBELLADONNA, CUPRUM ACETICUM, DROSERA, GRINDELIA, IPECAC, LOBELIA INFLATA, NAPHTHALINUM, YERBA SANTATotal Operations Management LLC DBA:Bestmade Natural Products Micro54103c3b-1974-b550-e063-6394a90a31452026-06-12WarningsExact identifier
ndc (package): 82969-2313-1
ndc (product): 82969-2313
ndc11 (package): 82969231301
spl id: 54103d93-93ef-b0a7-e063-6394a90a5dab
spl set id: 54103c3b-1974-b550-e063-6394a90a3145
BM BM13 DROPSBELLADONNA, CUPRUM ACETICUM, DROSERA, GRINDELIA, IPECAC, LOBELIA INFLATA, NAPHTHALINUM, YERBA SANTABM Private Limited53e86e23-8619-aef7-e063-6394a90ac38e2026-06-10WarningsExact identifier
ndc (product): 85816-2013

Reported adverse events (FAERS/openFDA)#

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