arnica aurum 20/30

Generic: arnica aurum 20/30

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

Drug Facts

Product Profile

Brand Name arnica aurum 20/30
Generic Name arnica aurum 20/30
Labeler uriel pharmacy inc.
Dosage Form LIQUID
Routes
ORAL
Active Ingredients

arnica montana 20 [hp_X]/mL, gold 30 [hp_X]/mL, hyoscyamus niger leaf 4 [hp_X]/mL, onopordum acanthium flower 3 [hp_X]/mL, primula veris flower 3 [hp_X]/mL

Manufacturer
Uriel Pharmacy Inc.

Identifiers & Regulatory

Product NDC 48951-1106
Product ID 48951-1106_44840be2-b7bb-ba38-e063-6394a90a0e38
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 489511106
Hyphenated Format 48951-1106

Supplemental Identifiers

UNII
O80TY208ZW 79Y1949PYO 32IT7G8BAW AP97AUF88E W5BET37294
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 arnica aurum 20/30 (source: ndc)
Generic Name arnica aurum 20/30 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 20 [hp_X]/mL
  • 30 [hp_X]/mL
  • 4 [hp_X]/mL
  • 3 [hp_X]/mL
source: ndc
Packaging
  • 10 AMPULE in 1 BOX (48951-1106-1) / 1 mL in 1 AMPULE
source: ndc

Packages (1)

48951-1106-1 10 AMPULE in 1 BOX (48951-1106-1) / 1 mL in 1 AMPULE

Ingredients (5)

arnica montana (20 [hp_X]/mL) gold (30 [hp_X]/mL) hyoscyamus niger leaf (4 [hp_X]/mL) onopordum acanthium flower (3 [hp_X]/mL) primula veris flower (3 [hp_X]/mL)

Linked Drug Pages (1)

Arnica Aurum 20/30 ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "44840be2-b7bb-ba38-e063-6394a90a0e38", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["O80TY208ZW", "79Y1949PYO", "32IT7G8BAW", "AP97AUF88E", "W5BET37294"], "spl_set_id": ["9ebdcfa6-f8b1-4a25-9008-e9f923ec9ffd"], "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": "10 AMPULE in 1 BOX (48951-1106-1)  / 1 mL in 1 AMPULE", "package_ndc": "48951-1106-1", "marketing_start_date": "20090901"}], "brand_name": "Arnica Aurum 20/30", "product_id": "48951-1106_44840be2-b7bb-ba38-e063-6394a90a0e38", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "48951-1106", "generic_name": "Arnica Aurum 20/30", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Arnica Aurum 20/30", "active_ingredients": [{"name": "ARNICA MONTANA", "strength": "20 [hp_X]/mL"}, {"name": "GOLD", "strength": "30 [hp_X]/mL"}, {"name": "HYOSCYAMUS NIGER LEAF", "strength": "4 [hp_X]/mL"}, {"name": "ONOPORDUM ACANTHIUM FLOWER", "strength": "3 [hp_X]/mL"}, {"name": "PRIMULA VERIS FLOWER", "strength": "3 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}