OXYRUB MAX PAIN RELIEF CREAM, 2OZ- menthol, methyl salicylate cream 
Healthy Directions, LLC

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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OxyRub MAX Pain Relief Cream, 2oz

Drug Facts 

Active Ingredients 

Methol (2.5%)

Methyl Salicylate (10%)

Purpose

Topical Analgesic 

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with: 

Warnings

For external use only:Use only as directed

Do not use

  • with a heating pad, may blister skin
  • on open wounds or damaged skin 

Ask a doctor before use if you have redness over the affected area

When using this product

  • avoid contact with eyes 
  • do not bandage tightly

Stop use and consult a doctor if

  • skin redness or excessive skin irritation developments
  • condition worsens or symptoms persist for more than 7 days 
  • symptoms clear up and occur again in a few days 

Keep out of reach of children. 

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

Directions

Adults and children 12 years of age and older: Apply to affected area no

more than 3-4 times daily. Children under 12 years of age: Consult a doctor. 

Other information 

Store at room termperature. For Lot Number and Expiration Date, see bottom of the carton. 

Inactive ingredients C13-14, Insoaraffin,

Citrus Aurantium Dulcis (Organe) Oil,

Ehtylhexlglycerin, Eucalyptus Globulus Oil,

Glyceryl Stearate, Laureth-7, Oxidized Corn

Oil, PEG-100 Stearate, Phenoxyethanol,

Polyacrylamide, Polysorbate-20, Water 

Dr. Perigolizzi 

OxyRub 

MAX

Pain Relief Cream

Extra Strength 

Muscle & Joint Pain Relief 

Rapidly Absorbed 

Deep Penetrating 

Distributed by 

HEALTHY DIRECTIONS 

Bethesda, MD 20817

healthydirections.com

OxyRubMAX2oz

OXYRUB MAX PAIN RELIEF  CREAM, 2OZ
menthol, methyl salicylate cream
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70015-650
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL25.0 mg  in 1 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE100.0 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
C13-16 ISOPARAFFIN (UNII: LED42LZG6O)  
ORANGE OIL (UNII: AKN3KSD11B)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
LAURETH-7 (UNII: Z95S6G8201)  
CORN OIL (UNII: 8470G57WFM)  
PEG-100 STEARATE (UNII: YD01N1999R)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
POLYACRYLAMIDE (CROSSLINKED; 0.01-0.2 MOLE PERCENT BISACRYLAMIDE) (UNII: RHA9LWJ494)  
POLYSORBATE 20 (UNII: 7T1F30V5YH)  
WATER (UNII: 059QF0KO0R)  
Product Characteristics
ColorwhiteScore    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70015-650-021 in 1 CARTON06/01/2017
157 g in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34806/01/2017
Labeler - Healthy Directions, LLC (150261183)
Establishment
NameAddressID/FEIBusiness Operations
Pure Source, LLC080354456manufacture(70015-650)

Revised: 5/2017
Document Id: b8d79ecd-b1c0-461d-829b-2913dc48446f
Set id: 6fea637f-bf6f-455f-b3d0-416bca1b811d
Version: 1
Effective Time: 20170502
 
Healthy Directions, LLC