FDA.reportPublic FDA data

BM HOMEOPATHIC LIQUID PASSI VALERIAN

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 01:01:12

Label at a glance#

ProductPASSI VALERIAN
Active ingredientARNICA MONTANA, GELSEMIUM SEMPERVIRENS ROOT, VALERIAN, DIBASIC POTASSIUM PHOSPHATE, MOSCHUS MOSCHIFERUS MUSK SAC RESIN, PASSIFLORA INCARNATA FLOWERING TOP
Label structure9 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

25-30 drops in half cup of water an hour before going to bed

OTC - ACTIVE INGREDIENT SECTION

arnica montana, gelsemium, kali phos, moschus, passiflora, valeriana

INACTIVE INGREDIENT SECTION

ALCOHOL

INDICATIONS & USAGE SECTION

A traditional homoeopathic formula for the temporary relieve of sleep disturbances due to symptoms of mild anxiety, for detail please read the enclosed package.
(Product information leaflet).

OTC - PURPOSE SECTION

A traditional homoeopathic formula for the temporary relieve of sleep disturbances due to symptoms of mild anxiety, 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

Passi ValerianPassi Valerian

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
Data codeQR CodeBM Homoeopathic Pharmaceuticals NP Passi Valerian 30mL (Drops) A traditional homoeopathic formula for the temporary relieve of sleep disturbances due to symptoms of mild anxiety. DRAP Mfg. Enl. # 0041, Prod. Enl. # 0041880992Passi Valerian.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product 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
85816-601285816-6012-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Name, UNII, Kind table
NameUNIIKind
ARNICA MONTANAO80TY208ZWACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
VALERIANJWF5YAW3QWACTIB
DIBASIC POTASSIUM PHOSPHATECI71S98N1ZACTIB
MOSCHUS MOSCHIFERUS MUSK SAC RESIN8KFK4W7KP7ACTIB
PASSIFLORA INCARNATA FLOWERING TOPCLF5YFS11OACTIB
ALCOHOL3K9958V90MIACT

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
3b3ae7ec-48e9-49b4-e063-6394a90a97893b3ae7ec-48e8-49b4-e063-6394a90a97892025-07-31WarningsExact identifier
spl set id: 3b3ae7ec-48e8-49b4-e063-6394a90a9789

Reported adverse events (FAERS/openFDA)#

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