BMNP-LABEL EQUISETUM HYEMALE 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 01:01:12

Label at a glance#

ProductBMNP EQUISETUM HYEMALE
Active ingredientEQUISETUM HYEMALE 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: frequent urge to urinate, persistent bladder pressure, discomfort after urination, nighttime urinary symptoms

OTC - PURPOSE SECTION

Equisetum Hyemale 30C (HPUS)......urinary irritation, frequent and painful urination, bladder pressure, nighttime aggravation

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

OTC - ACTIVE INGREDIENT SECTION

EQUISETUM HYEMALE 30C

INACTIVE INGREDIENT SECTION

Sucrose, PVP K 30, Magnesium Stearate, Aerosil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package 2

Equisetum HyemEquisetum Hyem

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codefastremedypicker.com/-_Equisetum Hyem 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
82969-527782969-5277-1, 82969-5277-2

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.