UNIVERSAL COCOA BUTTER 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 COCOA BUTTER SCENT PETROLEUM
Generic name: WHITE PETROLEUM
Manufacturer: Universal Distribution Center LLC
Product type: HUMAN OTC DRUG
SPL set ID: ec688073-6577-6cf9-e053-2a95a90a631d
SPL ID: 64bcc5b6-d1d8-4292-a0ee-e6a4132c1652
Version: 2
Effective date: 2024-12-04
Source export date: 2026-09-28
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/663999d0fe1757c1e2cd13a4799d76d875f663e0bc57701092264ebe7febfc18/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:25:01

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 COCOA BUTTER SCENT PETROLEUM	openfda.brand_name
generic name		WHITE PETROLEUM	openfda.generic_name
manufacturer name		Universal Distribution Center LLC	openfda.manufacturer_name
ndc	package	52000-119-03	openfda.package_ndc
ndc	package	52000-119-02	openfda.package_ndc
ndc	package	52000-119-01	openfda.package_ndc
ndc	package	52000-119-04	openfda.package_ndc
ndc	product	52000-119	openfda.product_ndc
ndc11	package	52000011902	derived:openfda.package_ndc
ndc11	package	52000011903	derived:openfda.package_ndc
ndc11	package	52000011904	derived:openfda.package_ndc
ndc11	package	52000011901	derived:openfda.package_ndc
rxcui		1148414	openfda.rxcui
spl id		64bcc5b6-d1d8-4292-a0ee-e6a4132c1652	id
spl set id		ec688073-6577-6cf9-e053-2a95a90a631d	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.