CeraVe Developed with Dermatologists Itch Relief Moisturizing

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: CeraVe Developed with Dermatologists Itch Relief Moisturizing
Generic name: PRAMOXINE HYDROCHLORIDE
Manufacturer: L'Oreal USA Products Inc
Product type: HUMAN OTC DRUG
SPL set ID: c6a0880e-fc16-46e9-8314-c56c9d15bf31
SPL ID: 61f5c62e-a06b-4e06-868a-db8df7fcb16b
Version: 5
Effective date: 2023-12-31
Source export date: 2026-10-30
Source partition: 1
Source file: https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-30/772d0e4623a189b47f3ab71d7d51f9b3c89c5526f4cf3d218e1c921bb964b80c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run: 20261102T182004Z
Imported at: 2026-11-02 18:28:22

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 · 15 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		CeraVe Developed with Dermatologists Itch Relief Moisturizing	openfda.brand_name
generic name		PRAMOXINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		L'Oreal USA Products Inc	openfda.manufacturer_name
ndc	package	49967-512-02	openfda.package_ndc
ndc	package	49967-512-01	openfda.package_ndc
ndc	package	49967-512-03	openfda.package_ndc
ndc	product	49967-512	openfda.product_ndc
ndc11	package	49967051202	derived:openfda.package_ndc
ndc11	package	49967051203	derived:openfda.package_ndc
ndc11	package	49967051201	derived:openfda.package_ndc
rxcui		1052684	openfda.rxcui
spl id		61f5c62e-a06b-4e06-868a-db8df7fcb16b	id
spl set id		c6a0880e-fc16-46e9-8314-c56c9d15bf31	set_id
unii		88AYB867L5	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 Do not use on deep or puncture wounds animal bites serious burns 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.