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: 13ce57d0-b1c5-4685-ad7d-a562d9d8fc86
SPL ID: ea7e8fa8-1b1c-46e5-88e5-b6a5f853ffc8
Version: 9
Effective date: 2026-05-12
Source export date: 2026-09-28
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:47:30

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 · 16 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	49967-970-04	openfda.package_ndc
ndc	package	49967-970-01	openfda.package_ndc
ndc	package	49967-970-02	openfda.package_ndc
ndc	package	49967-970-03	openfda.package_ndc
ndc	product	49967-970	openfda.product_ndc
ndc11	package	49967097003	derived:openfda.package_ndc
ndc11	package	49967097001	derived:openfda.package_ndc
ndc11	package	49967097002	derived:openfda.package_ndc
ndc11	package	49967097004	derived:openfda.package_ndc
spl id		ea7e8fa8-1b1c-46e5-88e5-b6a5f853ffc8	id
spl set id		13ce57d0-b1c5-4685-ad7d-a562d9d8fc86	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.