oxalis 20%
Generic: oxalis 20%
Labeler: uriel pharmcy, incDrug Facts
Product Profile
Brand Name
oxalis 20%
Generic Name
oxalis 20%
Labeler
uriel pharmcy, inc
Dosage Form
OINTMENT
Routes
Active Ingredients
oxalis stricta whole 1 [hp_X]/g
Manufacturer
Identifiers & Regulatory
Product NDC
48951-7221
Product ID
48951-7221_3b52ff8d-4b88-d598-e063-6294a90aebd0
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
489517221
Hyphenated Format
48951-7221
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
oxalis 20% (source: ndc)
Generic Name
oxalis 20% (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 [hp_X]/g
Packaging
- 60 g in 1 TUBE (48951-7221-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "3b52ff8d-4b88-d598-e063-6294a90aebd0", "openfda": {"unii": ["3STW243384"], "spl_set_id": ["3b52ff8d-4b87-d598-e063-6294a90aebd0"], "manufacturer_name": ["Uriel Pharmcy, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 g in 1 TUBE (48951-7221-5)", "package_ndc": "48951-7221-5", "marketing_start_date": "20090901"}], "brand_name": "Oxalis 20%", "product_id": "48951-7221_3b52ff8d-4b88-d598-e063-6294a90aebd0", "dosage_form": "OINTMENT", "product_ndc": "48951-7221", "generic_name": "Oxalis 20%", "labeler_name": "Uriel Pharmcy, Inc", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Oxalis 20%", "active_ingredients": [{"name": "OXALIS STRICTA WHOLE", "strength": "1 [hp_X]/g"}], "marketing_category": "UNAPPROVED HOMEOPATHIC", "marketing_start_date": "20090901", "listing_expiration_date": "20261231"}