UNIVERSAL LAVENDER SCENT 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 LAVENDER SCENT PETROLEUM
Generic name: WHITE PETROLEUM
Manufacturer: Universal Distribution Center LLC
Product type: HUMAN OTC DRUG
SPL set ID: 066b1313-aed8-9436-e063-6294a90a2b11
SPL ID: 498e79b1-89f7-e051-e063-6294a90ae14d
Version: 3
Effective date: 2026-01-29
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:06:06

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 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		UNIVERSAL LAVENDER SCENT PETROLEUM	openfda.brand_name
generic name		WHITE PETROLEUM	openfda.generic_name
manufacturer name		Universal Distribution Center LLC	openfda.manufacturer_name
ndc	package	52000-150-02	openfda.package_ndc
ndc	package	52000-150-01	openfda.package_ndc
ndc	package	52000-150-03	openfda.package_ndc
ndc	package	52000-150-04	openfda.package_ndc
ndc	product	52000-150	openfda.product_ndc
ndc11	package	52000015001	derived:openfda.package_ndc
ndc11	package	52000015003	derived:openfda.package_ndc
ndc11	package	52000015004	derived:openfda.package_ndc
ndc11	package	52000015002	derived:openfda.package_ndc
rxcui		1148414	openfda.rxcui
spl id		498e79b1-89f7-e051-e063-6294a90ae14d	id
spl set id		066b1313-aed8-9436-e063-6294a90a2b11	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.