strophanthus aurum

Generic: strophanthus aurum

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

Drug Facts

Product Profile

Brand Name strophanthus aurum
Generic Name strophanthus aurum
Labeler uriel pharmacy inc.
Dosage Form PELLET
Routes
ORAL
Active Ingredients

antimony 8 [hp_X]/1, gold 10 [hp_X]/1, hyoscyamus niger leaf 4 [hp_X]/1, onopordum acanthium flower 3 [hp_X]/1, primula veris flower 3 [hp_X]/1, strophanthus kombe whole 5 [hp_X]/1

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-8217
Product ID 48951-8217_3894ade6-f3f7-ec17-e063-6294a90a6b05
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 489518217
Hyphenated Format 48951-8217

Supplemental Identifiers

UNII
9IT35J3UV3 79Y1949PYO 32IT7G8BAW AP97AUF88E W5BET37294 Q1O0N901S4
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 strophanthus aurum (source: ndc)
Generic Name strophanthus aurum (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 8 [hp_X]/1
  • 10 [hp_X]/1
  • 4 [hp_X]/1
  • 3 [hp_X]/1
  • 5 [hp_X]/1
source: ndc
Packaging
  • 1350 PELLET in 1 BOTTLE, GLASS (48951-8217-2)
source: ndc

Packages (1)

Ingredients (6)

antimony (8 [hp_X]/1) gold (10 [hp_X]/1) hyoscyamus niger leaf (4 [hp_X]/1) onopordum acanthium flower (3 [hp_X]/1) primula veris flower (3 [hp_X]/1) strophanthus kombe whole (5 [hp_X]/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3894ade6-f3f7-ec17-e063-6294a90a6b05", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["9IT35J3UV3", "79Y1949PYO", "32IT7G8BAW", "AP97AUF88E", "W5BET37294", "Q1O0N901S4"], "spl_set_id": ["5a10efe0-d107-463e-a2b9-55c0e538640c"], "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 (48951-8217-2)", "package_ndc": "48951-8217-2", "marketing_start_date": "20090901"}], "brand_name": "Strophanthus Aurum", "product_id": "48951-8217_3894ade6-f3f7-ec17-e063-6294a90a6b05", "dosage_form": "PELLET", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "48951-8217", "generic_name": "Strophanthus Aurum", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Strophanthus Aurum", "active_ingredients": [{"name": "ANTIMONY", "strength": "8 [hp_X]/1"}, {"name": "GOLD", "strength": "10 [hp_X]/1"}, {"name": "HYOSCYAMUS NIGER LEAF", "strength": "4 [hp_X]/1"}, {"name": "ONOPORDUM ACANTHIUM FLOWER", "strength": "3 [hp_X]/1"}, {"name": "PRIMULA VERIS FLOWER", "strength": "3 [hp_X]/1"}, {"name": "STROPHANTHUS KOMBE WHOLE", "strength": "5 [hp_X]/1"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}