ZPOL ULTRA- menthol, methyl salicylate cream 
Laboratorios Zepol S.A.

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Zpol Ultra

Drug Facts

Active ingredients

Menthol 4%Methyl Salicylate 10%

Purpose

Active IngredientsPurpose
Menthol 2.84%Topical Analgesic
Methyl salicylate 18.24%Topical Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, bruises, and sprains.

Warnings

For external use only.

When using this product

Do not apply to wounds or damaged skin

Do not bandage tightly

Avoid contact with eyes

Do not use with a heating pad

Stop use and ask a doctor if

condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days.

If pregnant or breast-feeding

, ask a health professional before use.

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.

Children under 2 years of age: Do not use, consult a doctor.

Other information

Store between 20-25°C (68-77°F).

Inactive ingredients

Allantoin, benzoic acid, cetearyl alcohol, cetearyl glucoside, pheonoxyethanol, stearic acid, water.

Questions?

Call toll free +506 (800)-937-6572 laboratorioszepol@zepolab.com

zpol ULTRA 1.02 Oz

NDC 55715-008-01

zpol ULTRA

MUSCULAR Topical analgesic cream

Net wt. 1.02 Oz

ZepoLAB

Manufactured by

Laboratorios Zepol, S.A.

Curridabat, San José,

Costa Rica, 11801

Product of Costa Rica

IN COSTA RICA CALL FRO FREE 800-937-6572

(800-SZEPOLSA)

Regional Customer Service:

laboratorioszepol@zepolab.com

www.zepolab.com

Tamper Evident: Do not use if seal undercap is broken or missing

EXTERNAL USE/OVER THE COUNTER Zpol ULTRA Cream

is a medicated cream, due to its components and texture it is recommended for the relief of muscle pain, bumps, sprains and sports injuries. It also relieves arthritic and rheumatic pain.

E

I

zpol ULTRA 2.08 Oz

NDC 55715-008-02

zpol ULTRA

Topical analgesic cream

2.08 Oz

ZepoLAB

Zpol ULTRA 4.02 Oz

NDC 55715-008-03

zpol ULTRA

Topical analgesic cream

4.02 Oz

ZepoLAB

ZPOL ULTRA 
menthol, methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55715-008
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL2.84 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE18.24 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
SORBITAN TRISTEARATE (UNII: 6LUM696811)  
CARBOMER (UNII: 0A5MM307FC)  
CETEARYL ALCOHOL (UNII: 2DMT128M1S)  
GLYCERYL STEARATE (UNII: 230OU9XXE4)  
PEG-40 STEARATE (UNII: ECU18C66Q7)  
CETEARETH-20 (UNII: YRC528SWUY)  
EUCALYPTOL (UNII: RV6J6604TK)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
TRIETHANOLAMINE (UNII: 9O3K93S3TK)  
THYMOL (UNII: 3J50XA376E)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:55715-008-0129 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/01/2025
2NDC:55715-008-0259 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/01/2025
3NDC:55715-008-03119 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product04/01/2025
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01704/01/2025
Labeler - Laboratorios Zepol S.A. (853070985)
Establishment
NameAddressID/FEIBusiness Operations
Laboratorios Zepol S.A.853070985manufacture(55715-008)

Revised: 3/2025
Document Id: 315525bd-c7a7-77aa-e063-6394a90a89bf
Set id: 1a1433a6-8d04-96df-e063-6394a90a987b
Version: 3
Effective Time: 20250327
 
Laboratorios Zepol S.A.