FDA.reportPublic FDA data

ProCure LanaCare

Manufacturer
Twin Med LLC
Effective date
2025-09-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:13:39

Label at a glance#

ProductProCure LanaCare
Active ingredientLANOLIN
Label structure7 sections

Indications and uses

Uses Temporarily protects minor cuts, scrapes, and burns Temporarily protects and helps relieve chafed, chapped or cracked skin Helps protect from the drying effects of wind and cold weather

Dosage and administration

apply as needed

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lanolin 50%

Purpose

OTC - PURPOSE SECTION

Skin Protectant

Uses

INDICATIONS & USAGE SECTION

Uses

  • Temporarily protects minor cuts, scrapes, and burns
  • Temporarily protects and helps relieve chafed, chapped or cracked skin
  • Helps protect from the drying effects of wind and cold weather

Warnings

WARNINGS SECTION

Warnings

For external use only

When using this product

OTC - WHEN USING SECTION

When using this product do not get into the eyes

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

OTC - DO NOT USE SECTION

Do not use on

  • deep or puncture wounds
  • animal bites
  • serious burns

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of accidental ingestion contact a physician or Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

apply as needed

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petrolatum, Mineral Oil, Water, Sorbitan Sesquioleate, Beeswax, Disodium EDTA, Lanolin Alcohol, Sodium Borate, Phenoxyethanol, Ethylhexylglycerin

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PCLS04 ImagePCLS04 Image

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1038957lanolin 50 % Topical CreamPSN1
1038957lanolin 500 MG/ML Topical CreamSCD1
1038957lanolin 50 % Topical CreamSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55681-026-04ProCure LanaCare113 g in 1 TUBECREAM1131
55681-026-05ProCure LanaCare5 g in 1 PACKETCREAM51
55681-026-12ProCure LanaCare340 g in 1 JARCREAM3401
55681-026-14ProCure LanaCare144 in 1 CARTONCREAM1441
55681-026-15ProCure LanaCare14.2 g in 1 PACKETCREAM14.21
55681-026-36ProCure LanaCare36 in 1 CARTONCREAM361
55681-026-45ProCure LanaCare128 g in 1 JARCREAM1281

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
55681-02655681-026-04, 55681-026-45, 55681-026-12, 55681-026-05, 55681-026-14, 55681-026-15, 55681-026-36

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
SORBITAN SESQUIOLEATE0W8RRI5W5AIACT
LANOLIN ALCOHOLS884C3FA9HEIACT
LANOLIN7EV65EAW6HACTIB
PETROLATUM4T6H12BN9UIACT
PHENOXYETHANOLHIE492ZZ3TIACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
SODIUM BORATE91MBZ8H3QOIACT
MINERAL OILT5L8T28FGPIACT
EDETATE DISODIUM7FLD91C86KIACT
WATER059QF0KO0RIACT
YELLOW WAX2ZA36H0S2VIACT

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ProCure LanaCareLANOLIN 50%Twin Med LLC3aabd4ea-107c-a02c-e063-6294a90aee072025-09-15WarningsExact identifier
ndc (package): 55681-026-15
ndc (package): 55681-026-05
ndc (package): 55681-026-04
ndc (package): 55681-026-36
ndc (package): 55681-026-45
ndc (package): 55681-026-14
ndc (package): 55681-026-12
ndc (product): 55681-026
ndc11 (package): 55681002615
ndc11 (package): 55681002636
ndc11 (package): 55681002645
ndc11 (package): 55681002605
ndc11 (package): 55681002604
ndc11 (package): 55681002614
ndc11 (package): 55681002612
spl id: 3aabd4ea-107d-a02c-e063-6294a90aee07
spl set id: 3aabd4ea-107c-a02c-e063-6294a90aee07

Reported adverse events (FAERS/openFDA)#

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