aurum 21x
Generic: aurum 21x
Labeler: uriel pharmacy inc.Drug Facts
Product Profile
Brand Name
aurum 21x
Generic Name
aurum 21x
Labeler
uriel pharmacy inc.
Dosage Form
LIQUID
Routes
Active Ingredients
gold 21 [hp_X]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
48951-1318
Product ID
48951-1318_48889afd-554b-a47f-e063-6394a90a9bb0
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2027-12-31
Marketing Start
2009-09-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Physiologic Effect
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
489511318
Hyphenated Format
48951-1318
Supplemental Identifiers
UNII
NUI
Packaging Origin
Original Packager
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
aurum 21x (source: ndc)
Generic Name
aurum 21x (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 21 [hp_X]/mL
Packaging
- 10 AMPULE in 1 BOX (48951-1318-1) / 1 mL in 1 AMPULE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "48889afd-554b-a47f-e063-6394a90a9bb0", "openfda": {"nui": ["N0000185508", "N0000175629", "N0000184306", "M0000728"], "unii": ["79Y1949PYO"], "spl_set_id": ["93f243c0-b963-9ea0-e053-2995a90aa852"], "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 (48951-1318-1) / 1 mL in 1 AMPULE", "package_ndc": "48951-1318-1", "marketing_start_date": "20090901"}], "brand_name": "Aurum 21X", "product_id": "48951-1318_48889afd-554b-a47f-e063-6394a90a9bb0", "dosage_form": "LIQUID", "pharm_class": ["Allergens [CS]", "Cell-mediated Immunity [PE]", "Increased Histamine Release [PE]", "Standardized Chemical Allergen [EPC]"], "product_ndc": "48951-1318", "generic_name": "Aurum 21X", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Aurum 21X", "active_ingredients": [{"name": "GOLD", "strength": "21 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20271231"}