Derma-e Eczema Relief

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: Derma-e Eczema Relief
Generic name: OATMEAL
Manufacturer: Topiderm, Inc
Product type: HUMAN OTC DRUG
SPL set ID: e1797f81-af4b-49e1-9906-dbfd904a282b
SPL ID: facf2f71-8433-436b-9d4d-85ef301c7699
Version: 2
Effective date: 2020-08-19
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:20:56

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Derma-e Eczema Relief	openfda.brand_name
generic name		OATMEAL	openfda.generic_name
manufacturer name		Topiderm, Inc	openfda.manufacturer_name
ndc	package	51326-870-04	openfda.package_ndc
ndc	product	51326-870	openfda.product_ndc
ndc11	package	51326087004	derived:openfda.package_ndc
rxcui		240651	openfda.rxcui
spl id		facf2f71-8433-436b-9d4d-85ef301c7699	id
spl set id		e1797f81-af4b-49e1-9906-dbfd904a282b	set_id
unii		8PI54V663Y	openfda.unii

Warnings cross-check#

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

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only When using this product Do not get into eyes Stop use and ask a doctor if Condition worsens Symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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