TRIDERMA BABY STUBBORN ECZEMA ITCH 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: TRIDERMA BABY STUBBORN ECZEMA ITCH RELIEF
Generic name: COLLOIDAL OATMEAL
Manufacturer: Genuine Aloe Virgin Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f5a83e98-da32-49ae-b81d-4279af4b154c
SPL ID: 498d0d4c-7d48-5ff0-e063-6394a90ad849
Version: 6
Effective date: 2026-01-29
Source export date: 2026-09-28
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/f7d2b6e3f8600cd856280ab55a9c6fa54a642647191d164f9d1110e89f3f4097/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:14:57

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		505G(a)(3)	openfda.application_number
brand name		TRIDERMA BABY STUBBORN ECZEMA ITCH RELIEF	openfda.brand_name
generic name		COLLOIDAL OATMEAL	openfda.generic_name
manufacturer name		Genuine Aloe Virgin Corporation	openfda.manufacturer_name
ndc	package	10738-069-25	openfda.package_ndc
ndc	package	10738-069-45	openfda.package_ndc
ndc	package	10738-069-40	openfda.package_ndc
ndc	package	10738-069-20	openfda.package_ndc
ndc	product	10738-069	openfda.product_ndc
ndc11	package	10738006940	derived:openfda.package_ndc
ndc11	package	10738006925	derived:openfda.package_ndc
ndc11	package	10738006920	derived:openfda.package_ndc
ndc11	package	10738006945	derived:openfda.package_ndc
rxcui		1654721	openfda.rxcui
spl id		498d0d4c-7d48-5ff0-e063-6394a90ad849	id
spl set id		f5a83e98-da32-49ae-b81d-4279af4b154c	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 Do not use •on deep puncture wounds •on infections •on lacerations When using this product •avoid contact with eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if •condition worsens or does not improve within 7 days Keep out of reach of children. If swallowed get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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