bambusa aurum (48951-2009)

Drug Facts

Product Profile

Brand Name bambusa aurum

Generic Name bambusa aurum

Labeler uriel pharmacy inc.

Dosage Form PELLET

Routes

ORAL

Active Ingredients

arnica montana 20 [hp_X]/1, bambusa vulgaris whole 6 [hp_X]/1, bos taurus intervertebral disc 6 [hp_X]/1, formica rufa 5 [hp_X]/1, gold 16 [hp_X]/1, rosmarinus officinalis flowering top 6 [hp_X]/1, silicon dioxide 12 [hp_X]/1, stachys officinalis 6 [hp_X]/1

Manufacturer

Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-2009

Product ID 48951-2009_38954153-3a4d-08a2-e063-6394a90a2eea

Product Type HUMAN OTC DRUG

Marketing Category UNAPPROVED HOMEOPATHIC

Listing Expiration 2026-12-31

Marketing Start 2009-09-01

Pharmacologic Class

Established (EPC)

standardized chemical allergen [epc]

Chemical Structure

allergens [cs]

Physiologic Effect

increased histamine release [pe] cell-mediated immunity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489512009

Hyphenated Format 48951-2009

Supplemental Identifiers

UNII

O80TY208ZW WCD45M1BSK 0A04Z76C13 55H0W83JO5 79Y1949PYO 8JM482TI79 ETJ7Z6XBU4 UO9989Y17N

NUI

N0000185508 N0000175629 N0000184306 M0000728

Packaging Origin

Original Packager

true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name bambusa aurum (source: ndc)

Generic Name bambusa aurum (source: ndc)

Routes

ORAL

source: ndc

Resolved Composition

Strengths

20 [hp_X]/1
6 [hp_X]/1
5 [hp_X]/1
16 [hp_X]/1
12 [hp_X]/1

source: ndc

Packaging

1350 PELLET in 1 BOTTLE, GLASS (48951-2009-2)

source: ndc

Packages (1)

48951-2009-2 1350 PELLET in 1 BOTTLE, GLASS (48951-2009-2)

Ingredients (8)

arnica montana (20 [hp_X]/1) bambusa vulgaris whole (6 [hp_X]/1) bos taurus intervertebral disc (6 [hp_X]/1) formica rufa (5 [hp_X]/1) gold (16 [hp_X]/1) rosmarinus officinalis flowering top (6 [hp_X]/1) silicon dioxide (12 [hp_X]/1) stachys officinalis (6 [hp_X]/1)

Linked Drug Pages (1)

Bambusa Aurum ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload

{"route": ["ORAL"], "spl_id": "38954153-3a4d-08a2-e063-6394a90a2eea", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["O80TY208ZW", "WCD45M1BSK", "0A04Z76C13", "55H0W83JO5", "79Y1949PYO", "8JM482TI79", "ETJ7Z6XBU4", "UO9989Y17N"], "spl_set_id": ["43f3dd30-701f-4fa4-9743-d10051c6e6d4"], "pharm_class_cs": ["Allergens [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]"], "pharm_class_epc": ["Standardized Chemical Allergen [EPC]"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1350 PELLET in 1 BOTTLE, GLASS (48951-2009-2)", "package_ndc": "48951-2009-2", "marketing_start_date": "20090901"}], "brand_name": "Bambusa Aurum", "product_id": "48951-2009_38954153-3a4d-08a2-e063-6394a90a2eea", "dosage_form": "PELLET", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "48951-2009", "generic_name": "Bambusa Aurum", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Bambusa Aurum", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "20 [hp_X]/1"}, {"name": "BAMBUSA VULGARIS WHOLE", "strength": "6 [hp_X]/1"}, {"name": "BOS TAURUS INTERVERTEBRAL DISC", "strength": "6 [hp_X]/1"}, {"name": "FORMICA RUFA", "strength": "5 [hp_X]/1"}, {"name": "GOLD", "strength": "16 [hp_X]/1"}, {"name": "ROSMARINUS OFFICINALIS FLOWERING TOP", "strength": "6 [hp_X]/1"}, {"name": "SILICON DIOXIDE", "strength": "12 [hp_X]/1"}, {"name": "STACHYS OFFICINALIS", "strength": "6 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}