UNIVERSAL PURE PETROLEUM COCOA BUTTER SCENTED

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 PURE PETROLEUM COCOA BUTTER SCENTED
Generic name: WHITE PETROLEUM
Manufacturer: Universal Distribution Center LLC
Product type: HUMAN OTC DRUG
SPL set ID: 649e571f-0cd6-41e4-b31f-c818f94fb01d
SPL ID: ea88a572-836d-4188-b66d-e8ce34e6c90f
Version: 5
Effective date: 2024-10-15
Source export date: 2026-11-06
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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 06:46:39

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 · 29 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		UNIVERSAL PURE PETROLEUM COCOA BUTTER SCENTED	openfda.brand_name
generic name		WHITE PETROLEUM	openfda.generic_name
manufacturer name		Universal Distribution Center LLC	openfda.manufacturer_name
ndc	package	52000-007-27	openfda.package_ndc
ndc	package	52000-007-24	openfda.package_ndc
ndc	package	52000-007-22	openfda.package_ndc
ndc	package	52000-007-20	openfda.package_ndc
ndc	package	52000-007-21	openfda.package_ndc
ndc	package	52000-007-23	openfda.package_ndc
ndc	package	52000-007-26	openfda.package_ndc
ndc	package	52000-007-25	openfda.package_ndc
ndc	package	52000-007-19	openfda.package_ndc
ndc	package	52000-007-28	openfda.package_ndc
ndc	product	52000-007	openfda.product_ndc
ndc11	package	52000000723	derived:openfda.package_ndc
ndc11	package	52000000725	derived:openfda.package_ndc
ndc11	package	52000000728	derived:openfda.package_ndc
ndc11	package	52000000720	derived:openfda.package_ndc
ndc11	package	52000000727	derived:openfda.package_ndc
ndc11	package	52000000719	derived:openfda.package_ndc
ndc11	package	52000000722	derived:openfda.package_ndc
ndc11	package	52000000726	derived:openfda.package_ndc
ndc11	package	52000000721	derived:openfda.package_ndc
ndc11	package	52000000724	derived:openfda.package_ndc
rxcui		204754	openfda.rxcui
spl id		ea88a572-836d-4188-b66d-e8ce34e6c90f	id
spl set id		649e571f-0cd6-41e4-b31f-c818f94fb01d	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

Warning s 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.