Resurfix Plus

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: Resurfix Plus
Generic name: PETROLATUM
Manufacturer: Topiderm, Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f100f43d-6ace-4c3a-9c85-640c0ab2e360
SPL ID: 08943c30-5564-45c7-8a9f-0eb705b2a3ae
Version: 4
Effective date: 2019-11-19
Source export date: 2026-09-28
Source partition: 13
Source file: https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:34:48

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 · 10 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		Resurfix Plus	openfda.brand_name
generic name		PETROLATUM	openfda.generic_name
manufacturer name		Topiderm, Inc.	openfda.manufacturer_name
ndc	package	51326-884-03	openfda.package_ndc
ndc	product	51326-884	openfda.product_ndc
ndc11	package	51326088403	derived:openfda.package_ndc
spl id		08943c30-5564-45c7-8a9f-0eb705b2a3ae	id
spl set id		f100f43d-6ace-4c3a-9c85-640c0ab2e360	set_id
unii		4T6H12BN9U	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 Not to be applied over puncture wounds, infections, or lacerations. If condition worsens or does not improve within 7 days, contact a physician. Keep out of reach of children. In case of accidental ingestion, seek professional assistance or contact a Poison Control Center immediately. For external use only, not to be swallowed. Avoid contact with eyes.

Reported adverse events (FAERS/openFDA)#

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