Porphose

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: Porphose
Generic name: COLLOIDAL OATMEAL TOPICAL SPRAY
Manufacturer: Porphose
Product type: HUMAN OTC DRUG
SPL set ID: 315951e0-899f-c968-e063-6294a90abe61
SPL ID: 315951e0-89a0-c968-e063-6294a90abe61
Version: 1
Effective date: 2025-03-27
Source export date: 2026-10-12
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:11:06

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		Porphose	openfda.brand_name
generic name		COLLOIDAL OATMEAL TOPICAL SPRAY	openfda.generic_name
manufacturer name		Porphose	openfda.manufacturer_name
ndc	package	85456-001-01	openfda.package_ndc
ndc	product	85456-001	openfda.product_ndc
ndc11	package	85456000101	derived:openfda.package_ndc
rxcui		2709427	openfda.rxcui
spl id		315951e0-89a0-c968-e063-6294a90abe61	id
spl set id		315951e0-899f-c968-e063-6294a90abe61	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 wounds, animal bites, or serious burns. When using this product do not get into eyes. If contact occurs, rinse thoroughly with water. Stop use and ask a doctor if condition worsens, symptoms persist, or new irritation occurs.

Reported adverse events (FAERS/openFDA)#

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