OxyRub Pro Pain Relief Cream, 4oz

Dosage form: cream
Ingredients: MENTHOL 25.0mg in 1g, METHYL SALICYLATE 100.0mg in 1g
Labeler: Healthy Directions, LLC
NDC code: 70015-655

Medically reviewed by Drugs.com. Last updated on Aug 5, 2024.

OxyRub PRO Pain Relief Cream, 4oz

Drug Facts

Active Ingredients

Menthol (2.5%)

Methyl Salicylate (10%)

Purpose

Topical Analgesic

Uses

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

simple backaches
arthritis
strains
sprains
bruises

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 develops
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 or crimp at end of tube.

Inactive ingredients C13-14 Isoparaffin,

Citrus Aurantium Dulcis (Orange) Oil,

Ethylhexylglycerin, Eucalyptus Globulus Oil,

Glyceryl Stearate, Laureth-7, Oxidized Corn

Oil, PEG-100 Stearate, Phenoxyethanol,

Polyacrylamide, Polysorbate-20, Water

Dr. Pergolizzi

OxyRub

PRO

Pain Relief Cream

PROFESSIONAL STRENGTH

MUSCLE & JOINT

PAIN RELIEF

RAPIDLY

ABSORBED

DEEP

PENETRATING

Net Wt. 4 oz (114 g)

Distributed by

HEALTHY DIRECTIONS

6710A Rockledge Drive, Suite 500

Bethesda, MD 20817

OXYRUB PRO PAIN RELIEF CREAM, 4OZ
menthol, methyl salicylate cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:70015-655
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (MENTHOL)	MENTHOL	25.0 mg in 1 g
METHYL SALICYLATE (SALICYLIC ACID)	METHYL SALICYLATE	100.0 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
ORANGE OIL
ETHYLHEXYLGLYCERIN
EUCALYPTUS OIL
GLYCERYL MONOSTEARATE
LAURETH-7
CORN OIL
PEG-100 STEARATE
PHENOXYETHANOL
POLYACRYLAMIDE (CROSSLINKED; 0.01-0.2 MOLE PERCENT BISACRYLAMIDE)
POLYSORBATE 20
WATER
C13-14 ISOPARAFFIN

Product Characteristics
Color	white	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description
1	NDC:70015-655-04	1 TUBE in 1 CARTON
1		114 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/01/2017

Labeler - Healthy Directions, LLC (150261183)

Establishment
Name	Address	ID/FEI	Operations
Pure Source, LLC		080354456	manufacture(70015-655)

Revised: 08/2017

Document Id: d417edfb-86ce-4554-b1ce-ce126af62abb

Set id: be26909d-afbb-4b89-a64a-fd130de223c7

Version: 1

Effective Time: 20170815

Healthy Directions, LLC

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

Medical Disclaimer