ProCure LanaCare

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: ProCure LanaCare
Generic name: LANOLIN 50%
Manufacturer: Twin Med LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3aabd4ea-107c-a02c-e063-6294a90aee07
SPL ID: 3aabd4ea-107d-a02c-e063-6294a90aee07
Version: 1
Effective date: 2025-09-15
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:17

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 · 23 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M016	openfda.application_number
brand name		ProCure LanaCare	openfda.brand_name
generic name		LANOLIN 50%	openfda.generic_name
manufacturer name		Twin Med LLC	openfda.manufacturer_name
ndc	package	55681-026-15	openfda.package_ndc
ndc	package	55681-026-05	openfda.package_ndc
ndc	package	55681-026-04	openfda.package_ndc
ndc	package	55681-026-36	openfda.package_ndc
ndc	package	55681-026-45	openfda.package_ndc
ndc	package	55681-026-14	openfda.package_ndc
ndc	package	55681-026-12	openfda.package_ndc
ndc	product	55681-026	openfda.product_ndc
ndc11	package	55681002615	derived:openfda.package_ndc
ndc11	package	55681002636	derived:openfda.package_ndc
ndc11	package	55681002645	derived:openfda.package_ndc
ndc11	package	55681002605	derived:openfda.package_ndc
ndc11	package	55681002604	derived:openfda.package_ndc
ndc11	package	55681002614	derived:openfda.package_ndc
ndc11	package	55681002612	derived:openfda.package_ndc
rxcui		1038957	openfda.rxcui
spl id		3aabd4ea-107d-a02c-e063-6294a90aee07	id
spl set id		3aabd4ea-107c-a02c-e063-6294a90aee07	set_id
unii		7EV65EAW6H	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 Warnings For external use only When using this product When using this product do not get into the eyes Stop use and ask a doctor if 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 Do not use on Do not use on deep or puncture wounds animal bites serious burns Keep out of reach of children Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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