UNIVERSAL ORIGINAL PETROLEUM

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: UNIVERSAL ORIGINAL PETROLEUM
Generic name: WHITE PETROLEUM
Manufacturer: Universal Distribution Center LLC
Product type: HUMAN OTC DRUG
SPL set ID: 47b8c720-ad1e-4ac7-ba73-872e409b38bf
SPL ID: e464a1a6-ac35-4949-abdb-40c19970a1fc
Version: 3
Effective date: 2023-11-17
Source export date: 2026-10-12
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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:26:52

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		M016	openfda.application_number
brand name		UNIVERSAL ORIGINAL PETROLEUM	openfda.brand_name
generic name		WHITE PETROLEUM	openfda.generic_name
manufacturer name		Universal Distribution Center LLC	openfda.manufacturer_name
ndc	package	52000-104-04	openfda.package_ndc
ndc	package	52000-104-02	openfda.package_ndc
ndc	package	52000-104-03	openfda.package_ndc
ndc	package	52000-104-01	openfda.package_ndc
ndc	product	52000-104	openfda.product_ndc
ndc11	package	52000010404	derived:openfda.package_ndc
ndc11	package	52000010403	derived:openfda.package_ndc
ndc11	package	52000010402	derived:openfda.package_ndc
ndc11	package	52000010401	derived:openfda.package_ndc
rxcui		1148414	openfda.rxcui
spl id		e464a1a6-ac35-4949-abdb-40c19970a1fc	id
spl set id		47b8c720-ad1e-4ac7-ba73-872e409b38bf	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 For External Use Only. Do not use over deep or puncture wounds, infections or lacerations. Ask a doctor. When using this product avoid contact with eyes. Stop use and ask 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.