BM HOMEOPATHIC LIQUID RAU VISCUM

Manufacturer
BM Private Limited
Effective date
2026-10-26
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-29 01:01:08

Label at a glance#

ProductRAU VISCUM
Active ingredientCRATAEGUS LAEVIGATA WHOLE, VISCUM ALBUM FRUITING TOP, CILANTRO, PASSIFLORA INCARNATA FLOWERING TOP, NITROGLYCERIN, RAUWOLFIA SERPENTINA, GARLIC
Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

Dosage:
Adult:10-15 drops in half cup of water three times a day
Teenagers: half of the same

OTC - ACTIVE INGREDIENT SECTION

allium sat, coriandrum sat, crataegus oxy, glonoine, passiflora, rowolfia, viscum alb

INACTIVE INGREDIENT SECTION

Alcohol

INDICATIONS & USAGE SECTION

Help support to relieve the symptoms of high blood pressure, for detail please read the enclosed package.
(Product information leaflet).

OTC - PURPOSE SECTION

Help support to relieve the symptoms of high blood pressure, for detail please read the enclosed package.
(Product information leaflet).

CONTRAINDICATIONS SECTION

Care & contra-indications:
This is a homoeopathic remedy, no contra-indications are established.

WARNINGS SECTION

Precautions/storage:
Keep away from children and store at cool and dry place.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Precautions/storage:
Keep away from children and store at cool and dry place.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Rau viscumRau viscum

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR CodeBM Homoeopathic Pharmaceuticals BM's NP Rau viscum 30mL Drops Help support to relieve the symptoms of high blood pressure. DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041880994Rau-viscum.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
7480e90b-004b-ebe4-2243-4f2fefdd9e78Product name220260128
3f158398-73f2-4b90-47d1-5c60e8719a98Product name920250721
ca6149a6-ded3-9f17-6c41-3e88f2c0c9c0Product name220250117
00358076-c817-430b-b924-11d717dc307cProduct name120160718
669af5aa-14f3-3df7-f100-5f580ffd43c1Product name120140508
6ff3bab7-2dce-8bea-d7ce-54687f0c01fbProduct name120140508
8bb82a1c-d0d0-fc27-011f-172e545f0382Product name120140508
cb03406d-e223-80bb-67d8-be80f9b6a4f2Product name120140508

Products#

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

DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85816-601385816-6013-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-07-31full-release2026-06-01 02:34:35

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
3b3aafe4-716a-3b5f-e063-6394a90a9a6d3b3aafe4-7169-3b5f-e063-6394a90a9a6d2025-07-31WarningsExact identifier
spl set id: 3b3aafe4-7169-3b5f-e063-6394a90a9a6d

Reported adverse events (FAERS/openFDA)#

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