FDA.reportPublic FDA data

Bambusa Argentum

Manufacturer
Uriel Pharmacy Inc.
Effective date
2019-11-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:11:34

Label at a glance#

ProductBambusa Argentum
Active ingredientVISCUM ALBUM FRUITING TOP, STACHYS OFFICINALIS, ROSMARINUS OFFICINALIS FLOWERING TOP, FORMICA RUFA, BOS TAURUS INTERVERTEBRAL DISC, SILICON DIOXIDE, SILVER, ARNICA MONTANA, BAMBUSA VULGARIS WHOLE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR RECTAL USE ONLY.

DOSAGE & ADMINISTRATION SECTION

Insert 1 suppository as needed.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Viscum Mali 4X, Bambusa e nodo 8X, Betonica ex herba 8X, Rosmarinus ex herba 8X, Formica ex animale 9X, Disci intervert. 10X, Jasper 19X, Argentum met. 22X, Arnica e pl. tota 22X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Cocoa butter, Sorbitan monolaurate, Micronized silica gel

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

KEEP REFRIGERATED OR STORE IN
COOL, DRY PLACE. REFRIGERATE TO RESOLIDIFY.
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use. Do not use if safety seals on box are broken or missing.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bambusa Argentum SuppBambusa Argentum Supp

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-2135-12025-01-30C16284748780-12cef2736-853d-d83d-e063-dadaa90ab31fBambusa Argentum

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2135-1Bambusa Argentum10 in 1 BOXSUPPOSITORY102
48951-2135-1Bambusa Argentum2 g in 1 BLISTER PACKSUPPOSITORY22

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2135BAMBUSA ARGENTUM SUPPOSITORY [URIEL PHARMACY INC.]2Legacy NDC, 2 package rows20191121_6b51413d-74db-cfd2-e053-2a91aa0a5ad4.zip

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
48951-213548951-2135-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
VISCUM ALBUM FRUITING TOPBK9092J5MPACTIB
STACHYS OFFICINALISUO9989Y17NACTIB
ROSMARINUS OFFICINALIS FLOWERING TOP8JM482TI79ACTIB
FORMICA RUFA55H0W83JO5ACTIB
BOS TAURUS INTERVERTEBRAL DISC0A04Z76C13ACTIB
SILICON DIOXIDEETJ7Z6XBU4ACTIB
SILVER3M4G523W1GACTIB
ARNICA MONTANAO80TY208ZWACTIB
SORBITAN MONOLAURATE6W9PS8B71JIACT
COCOA BUTTER512OYT1CRRIACT
BAMBUSA VULGARIS WHOLEWCD45M1BSKACTIB

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 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
97b6f7c6-1b53-e4bd-e053-2a95a90afe816b51413d-74db-cfd2-e053-2a91aa0a5ad42019-11-19WarningsExact identifier
spl id: 97b6f7c6-1b53-e4bd-e053-2a95a90afe81
spl set id: 6b51413d-74db-cfd2-e053-2a91aa0a5ad4

Reported adverse events (FAERS/openFDA)#

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