White Petrolatum

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: White Petrolatum
Generic name: PETROLATUM
Manufacturer: Dynarex Corporation
Product type: HUMAN OTC DRUG
SPL set ID: 81f5092d-0632-bf47-e053-2991aa0ac563
SPL ID: 4ddba886-ec28-ef1e-e063-6394a90a3a86
Version: 16
Effective date: 2026-03-25
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 06:06:26

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 · 27 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		White Petrolatum	openfda.brand_name
generic name		PETROLATUM	openfda.generic_name
manufacturer name		Dynarex Corporation	openfda.manufacturer_name
ndc	package	67777-005-52	openfda.package_ndc
ndc	package	67777-005-11	openfda.package_ndc
ndc	package	67777-005-70	openfda.package_ndc
ndc	package	67777-005-51	openfda.package_ndc
ndc	package	67777-005-71	openfda.package_ndc
ndc	package	67777-005-10	openfda.package_ndc
ndc	package	67777-005-50	openfda.package_ndc
ndc	package	67777-005-01	openfda.package_ndc
ndc	package	67777-005-00	openfda.package_ndc
ndc	product	67777-005	openfda.product_ndc
ndc11	package	67777000550	derived:openfda.package_ndc
ndc11	package	67777000510	derived:openfda.package_ndc
ndc11	package	67777000551	derived:openfda.package_ndc
ndc11	package	67777000511	derived:openfda.package_ndc
ndc11	package	67777000552	derived:openfda.package_ndc
ndc11	package	67777000501	derived:openfda.package_ndc
ndc11	package	67777000571	derived:openfda.package_ndc
ndc11	package	67777000570	derived:openfda.package_ndc
ndc11	package	67777000500	derived:openfda.package_ndc
rxcui		204754	openfda.rxcui
spl id		4ddba886-ec28-ef1e-e063-6394a90a3a86	id
spl set id		81f5092d-0632-bf47-e053-2991aa0ac563	set_id
unii		B6E5W8RQJ4	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 on • Deep or puncture wounds • Animal bites • Serious burns When using this product • Avoid contact with eyes Stop use and ask a doctor if • Condition worsens • Symptoms last more than 7 days or clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-12222) right away.

Reported adverse events (FAERS/openFDA)#

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