urea
Generic: urea
Labeler: bantry pharma, llcDrug Facts
Product Profile
Brand Name
urea
Generic Name
urea
Labeler
bantry pharma, llc
Dosage Form
LOTION
Routes
Active Ingredients
urea 400 mg/g
Manufacturer
Identifiers & Regulatory
Product NDC
81542-201
Product ID
81542-201_36c18d8c-6e56-ad83-e063-6294a90a25fc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2021-09-07
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
81542201
Hyphenated Format
81542-201
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 (source: ndc)
Generic Name
urea (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 400 mg/g
Packaging
- 226.8 g in 1 BOTTLE (81542-201-08)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "36c18d8c-6e56-ad83-e063-6294a90a25fc", "openfda": {"unii": ["8W8T17847W"], "rxcui": ["351155"], "spl_set_id": ["cb6ddbfc-ea6a-0ddc-e053-2995a90aedc4"], "manufacturer_name": ["Bantry Pharma, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "226.8 g in 1 BOTTLE (81542-201-08)", "package_ndc": "81542-201-08", "marketing_start_date": "20210907"}], "brand_name": "UREA", "product_id": "81542-201_36c18d8c-6e56-ad83-e063-6294a90a25fc", "dosage_form": "LOTION", "product_ndc": "81542-201", "generic_name": "UREA", "labeler_name": "Bantry Pharma, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "UREA", "active_ingredients": [{"name": "UREA", "strength": "400 mg/g"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20210907", "listing_expiration_date": "20261231"}