stannum 30x
Generic: stannum 30x
Labeler: uriel pharmacy inc.Drug Facts
Product Profile
Brand Name
stannum 30x
Generic Name
stannum 30x
Labeler
uriel pharmacy inc.
Dosage Form
LIQUID
Routes
Active Ingredients
tin 30 [hp_X]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
48951-8356
Product ID
48951-8356_363833fa-b8d3-1093-e063-6394a90a77fc
Product Type
HUMAN OTC DRUG
Marketing Category
UNAPPROVED HOMEOPATHIC
Listing Expiration
2026-12-31
Marketing Start
2009-09-01
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
489518356
Hyphenated Format
48951-8356
Supplemental Identifiers
UNII
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
stannum 30x (source: ndc)
Generic Name
stannum 30x (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 30 [hp_X]/mL
Packaging
- 60 mL in 1 BOTTLE, DROPPER (48951-8356-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "363833fa-b8d3-1093-e063-6394a90a77fc", "openfda": {"unii": ["387GMG9FH5"], "spl_set_id": ["9454572b-643c-6cd1-e053-2a95a90ada1a"], "manufacturer_name": ["Uriel Pharmacy Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 mL in 1 BOTTLE, DROPPER (48951-8356-3)", "package_ndc": "48951-8356-3", "marketing_start_date": "20090901"}], "brand_name": "Stannum 30X", "product_id": "48951-8356_363833fa-b8d3-1093-e063-6394a90a77fc", "dosage_form": "LIQUID", "product_ndc": "48951-8356", "generic_name": "Stannum 30X", "labeler_name": "Uriel Pharmacy Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Stannum 30X", "active_ingredients": [{"name": "TIN", "strength": "30 [hp_X]/mL"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}