PROCURE LANACARE- lanolin 30% cream

ProCure LanaCare by

Drug Labeling and Warnings

ProCure LanaCare by is a Otc medication manufactured, distributed, or labeled by Twin Med LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active Ingredient

Lanolin 30%

Purpose

Skin Protectant

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

Warnings

Warnings

For external use only

When using this product

When using this product donot 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.

Directions

apply as needed

Inactive Ingredients

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

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

PROCURE LANACARE 
lanolin 30% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 55681-028
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
LANOLIN (UNII: 7EV65EAW6H) (LANOLIN - UNII:7EV65EAW6H)	LANOLIN	30 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)
LANOLIN ALCOHOLS (UNII: 884C3FA9HE)
PETROLATUM (UNII: 4T6H12BN9U)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM BORATE (UNII: 91MBZ8H3QO)
MINERAL OIL (UNII: T5L8T28FGP)
EDETATE DISODIUM (UNII: 7FLD91C86K)
WATER (UNII: 059QF0KO0R)
YELLOW WAX (UNII: 2ZA36H0S2V)

Product Characteristics
Color	yellow (Yellowish Color)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 55681-028-04	113 g in 1 TUBE; Type 0: Not a Combination Product	09/15/2025
2	NDC: 55681-028-14	144 in 1 CARTON	09/15/2025
2	NDC: 55681-028-05	5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M016	09/15/2025

Labeler - Twin Med LLC (009579330)