FDA.reportPublic FDA data

Bambusa Formica

Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-10-08
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
full-release
Hydrated at
2026-06-01 02:28:12

Label at a glance#

ProductBambusa Formica
Active ingredientBAMBUSA VULGARIS WHOLE, VISCUM ALBUM FRUITING TOP, FORMICA RUFA, TIN, EQUISETUM ARVENSE TOP, BOS TAURUS EYE
Label structure9 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Directions: FOR ORAL USE.

DOSAGE & ADMINISTRATION SECTION

Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Bambusa (Bamboo) 6X, Viscum Mali (Apple tree mistletoe) 6X, Formica (Red wood ant) 7X, Lens cristallina (Bovine crystalline lens of the eye) 8X, Stannum (Metallic tin) 10X, Equisetum (Horsetail) 15X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Water, Potassium nitrate, Boric acid, Silver sulfate, Rose water

Prepared using rhythmical processes

OTC - PURPOSE SECTION

Use: Temporary relief of headache.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

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 seal is broken or missing.

REFRIGERATE AFTER OPENING. USE WITHIN 30 DAYS OF OPENING.
Opened on:_________________

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858
Made by Uriel, East Troy, WI 53120
shopuriel.com

Lot:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Bambusa Formica 10mlBambusa Formica 10mlBambusa Formica 10ml LiquidBambusa Formica 10ml Liquid

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-2134-1Bambusa Formica10 mL in 1 BOTTLE, DROPPERLIQUID103
48951-2134-1Bambusa Formica1 in 1 BAGLIQUID13

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-2134BAMBUSA FORMICA LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20241010_92c2f4df-49e5-6345-e053-2a95a90a2531.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
48951-213448951-2134-1

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
ROSEMARY OIL8LGU7VM393IACT
SILVER SULFATE8QG6HV4ZPOIACT
BAMBUSA VULGARIS WHOLEWCD45M1BSKACTIB
VISCUM ALBUM FRUITING TOPBK9092J5MPACTIB
FORMICA RUFA55H0W83JO5ACTIB
TIN387GMG9FH5ACTIB
EQUISETUM ARVENSE TOP1DP6Y6B65ZACTIB
WATER059QF0KO0RIACT
BORIC ACIDR57ZHV85D4IACT
POTASSIUM NITRATERU45X2JN0ZIACT
BOS TAURUS EYEVTW461N43PACTIB

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
23f9c94d-15cb-23e0-e063-6394a90a622b92c2f4df-49e5-6345-e053-2a95a90a25312024-10-08WarningsExact identifier
spl id: 23f9c94d-15cb-23e0-e063-6394a90a622b
spl set id: 92c2f4df-49e5-6345-e053-2a95a90a2531

Reported adverse events (FAERS/openFDA)#

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