LIPROTEK- petrolatum, lidocaine ointment 
Unit Dose, Ltd.

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Liprotek

Uses:

TEMPORARY RELIEF OF PAIN and/or ITCHING FROM FEVER BLISTERS and COLD SORES

DRUG FACTS

Active Ingredient

Petrolatum (white) 61%

Lidocaine 0.6%

PURPOSE

Skin Protectant

External or Topical Analgesic

Uses:

TEMPORARY RELIEF OF PAIN AND/OR ITCHING FROM FEVER BLISTERS AND COLD SORES

WARNING:

Keep away from children.

Do not use

if allergic tp any of the ingredients. If condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days then discontinue use of this product and cunsult a doctor.

INGREDIENTS:

   Simmondisa Chinensis (Jojoba) Seed Oil, Lanolin, Beeswax, Ozokerite wax, Candelilla wax, Parafin, Aqua (Water), Polysorbate 60, 2-DG, Ethoxydiglycol, Menthol, Tocopheryl, Cholecalciferal, Retinyl Palmitate, Phytonadione

Package Labeling:

Outer

LIPROTEK 
petrolatum, lidocaine ointment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:67194-017
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
PETROLATUM (UNII: 4T6H12BN9U) (PETROLATUM - UNII:4T6H12BN9U) PETROLATUM610 mg  in 1 g
LIDOCAINE (UNII: 98PI200987) (LIDOCAINE - UNII:98PI200987) LIDOCAINE6 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
JOJOBA OIL (UNII: 724GKU717M)  
LANOLIN (UNII: 7EV65EAW6H)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
CERESIN (UNII: Q1LS2UJO3A)  
CANDELILLA WAX (UNII: WL0328HX19)  
PARAFFIN (UNII: I9O0E3H2ZE)  
WATER (UNII: 059QF0KO0R)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
2-DEOXYGLUCOSE (UNII: 9G2MP84A8W)  
DIETHYLENE GLYCOL MONOETHYL ETHER (UNII: A1A1I8X02B)  
MENTHOL (UNII: L7T10EIP3A)  
CHOLECALCIFEROL (UNII: 1C6V77QF41)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
PHYTONADIONE (UNII: A034SE7857)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:67194-017-014 g in 1 JAR; Type 0: Not a Combination Product01/21/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/21/2016
Labeler - Unit Dose, Ltd. (119080393)

Revised: 10/2023
Document Id: 0814dd5c-455c-739e-e063-6394a90ac8bc
Set id: 051cfa27-bd7c-4f8c-b3e6-03ee0b7a3aa5
Version: 5
Effective Time: 20231019
 
Unit Dose, Ltd.