urea 41%
Generic: urea
Labeler: puretek corporationDrug Facts
Product Profile
Brand Name
urea 41%
Generic Name
urea
Labeler
puretek corporation
Dosage Form
CREAM
Routes
Active Ingredients
urea 410 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
59088-489
Product ID
59088-489_da5d8eae-8d63-d354-e053-2995a90a7999
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2022-06-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
59088489
Hyphenated Format
59088-489
Supplemental Identifiers
RxCUI
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
urea 41% (source: ndc)
Generic Name
urea (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 410 mg/g
Packaging
- 227 g in 1 BOTTLE (59088-489-16)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "da5d8eae-8d63-d354-e053-2995a90a7999", "openfda": {"unii": ["8W8T17847W"], "rxcui": ["1436933"], "spl_set_id": ["da5d8eae-8d64-d354-e053-2995a90a7999"], "manufacturer_name": ["PureTek Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "227 g in 1 BOTTLE (59088-489-16)", "package_ndc": "59088-489-16", "marketing_start_date": "20220607"}], "brand_name": "Urea 41%", "product_id": "59088-489_da5d8eae-8d63-d354-e053-2995a90a7999", "dosage_form": "CREAM", "product_ndc": "59088-489", "generic_name": "Urea", "labeler_name": "PureTek Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Urea 41%", "active_ingredients": [{"name": "UREA", "strength": "410 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20220607", "listing_expiration_date": "20261231"}