BMNP-LABEL DROSERA ROTUNDIFOLIA 30C

Manufacturer
Total Operations Management LLC DBA:Bestmade Natural Products Micro | BM Private Limited
Effective date
2026-09-28
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-30 01:01:10

Label at a glance#

ProductBMNP DROSERA ROTUNDIFOLIA
Active ingredientDROSERA ROTUNDIFOLIA WHOLE
Label structure8 sections

Label contents#

Full prescribing information#

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.

DOSAGE & ADMINISTRATION SECTION

Use as directed.

Take with water, 3-4 times daily. Ages 12 and older: 2 pellets. Ages 3 to 11: 1 pellet. Ages below 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.

INDICATIONS & USAGE SECTION

Helps temporarily relieve: barking cough, throat irritation, nightime cough, throat tickling

OTC - PURPOSE SECTION

Drosera Rotundifolia 30C (HPUS)......barking cough, throat irritation, cough triggered by lying down or nighttime, tickling sensation in the throat

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

OTC - ACTIVE INGREDIENT SECTION

DROSERA ROTUNDIFOLIA 30C

INACTIVE INGREDIENT SECTION

Sucrose, PVP K 30, Magnesium Stearate, Aerosil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 2

Drosera Rot 30CDrosera Rot 30C

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codefastremedypicker.com/-_Drosera Rot 30C.jpg

Products#

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

DailyMed product names page 1 of 1 · 7 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
82969-527482969-5274-1, 82969-5274-2

Ingredients#

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

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

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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