betula argentum

Generic: betula argentum

Labeler: uriel pharmacy inc.
NDC Directory HUMAN OTC DRUG UNAPPROVED HOMEOPATHIC Inactive Finished

Drug Facts

Product Profile

Brand Name betula argentum
Generic Name betula argentum
Labeler uriel pharmacy inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

apis mellifera 3 [hp_X]/mL, arnica montana 17 [hp_X]/mL, betula pubescens bark 3 [hp_X]/mL, betula pubescens leaf 3 [hp_X]/mL, formica rufa 7 [hp_X]/mL, silver 8 [hp_X]/mL

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-2063
Product ID 48951-2063_3894ea71-3636-1458-e063-6394a90a08fd
Product Type HUMAN OTC DRUG
Marketing Category UNAPPROVED HOMEOPATHIC
Listing Expiration 2026-12-31
Marketing Start 2009-09-01

Pharmacologic Class

Established (EPC)
standardized insect venom allergenic extract [epc]
Chemical Structure
allergens [cs] bee venoms [cs]
Physiologic Effect
increased histamine release [pe] cell-mediated immunity [pe] increased igg production [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 489512063
Hyphenated Format 48951-2063

Supplemental Identifiers

UNII
7S82P3R43Z O80TY208ZW 3R504894L9 84SOH0O3OO 55H0W83JO5 3M4G523W1G
NUI
N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274

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 betula argentum (source: ndc)
Generic Name betula argentum (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 3 [hp_X]/mL
  • 17 [hp_X]/mL
  • 7 [hp_X]/mL
  • 8 [hp_X]/mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (48951-2063-1) / 1 mL in 1 AMPULE
source: ndc

Packages (1)

Ingredients (6)

apis mellifera (3 [hp_X]/mL) arnica montana (17 [hp_X]/mL) betula pubescens bark (3 [hp_X]/mL) betula pubescens leaf (3 [hp_X]/mL) formica rufa (7 [hp_X]/mL) silver (8 [hp_X]/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3894ea71-3636-1458-e063-6394a90a08fd", "openfda": {"nui": ["N0000185021", "N0000175629", "N0000184306", "N0000185001", "M0000728", "M0002274"], "unii": ["7S82P3R43Z", "O80TY208ZW", "3R504894L9", "84SOH0O3OO", "55H0W83JO5", "3M4G523W1G"], "spl_set_id": ["7f436fc5-0983-4ce3-9951-e68e395bcab0"], "pharm_class_cs": ["Allergens [CS]", "Bee Venoms [CS]"], "pharm_class_pe": ["Increased Histamine Release [PE]", "Cell-mediated Immunity [PE]", "Increased IgG Production [PE]"], "pharm_class_epc": ["Standardized Insect Venom Allergenic Extract [EPC]"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 BOX (48951-2063-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-2063-1", "marketing_start_date": "20090901"}], "brand_name": "Betula Argentum", "product_id": "48951-2063_3894ea71-3636-1458-e063-6394a90a08fd", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Bee Venoms [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Increased IgG Production [PE]", "Standardized Insect Venom Allergenic Extract [EPC]"], "product_ndc": "48951-2063", "generic_name": "Betula Argentum", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Betula Argentum", "active_ingredients": [{"name": "APIS MELLIFERA", "strength": "3 [hp_X]/mL"}, {"name": "ARNICA MONTANA", "strength": "17 [hp_X]/mL"}, {"name": "BETULA PUBESCENS BARK", "strength": "3 [hp_X]/mL"}, {"name": "BETULA PUBESCENS LEAF", "strength": "3 [hp_X]/mL"}, {"name": "FORMICA RUFA", "strength": "7 [hp_X]/mL"}, {"name": "SILVER", "strength": "8 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}