Urea 20

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Urea 20
Generic name: UREA
Manufacturer: AvPAK
Product type: HUMAN OTC DRUG
SPL set ID: e994fa05-a457-2555-e053-2a95a90ae83b
SPL ID: 48379414-bcb9-1797-e063-6394a90aa8fd
Version: 4
Effective date: 2026-01-12
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:26:52

Harmonized routes table
Harmonized routes
TOPICAL

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 9 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
brand name		Urea 20	openfda.brand_name
generic name		UREA	openfda.generic_name
manufacturer name		AvPAK	openfda.manufacturer_name
ndc	package	50268-820-85	openfda.package_ndc
ndc	product	50268-820	openfda.product_ndc
ndc11	package	50268082085	derived:openfda.package_ndc
spl id		48379414-bcb9-1797-e063-6394a90aa8fd	id
spl set id		e994fa05-a457-2555-e053-2a95a90ae83b	set_id
unii		8W8T17847W	openfda.unii

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

WARNINGS SECTION Caution: Do not apply to broken skin. If redness occurs, discontinue use. Avoid contact with eyes.

Adverse event summaries are temporarily unavailable. Other product information remains available.