DynaRub

Dosage form: cream
Ingredients: MENTHOL 10g in 100g, METHYL SALICYLATE 15g in 100g
Labeler: Dynarex Corporation
NDC code: 67777-113

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

1135 - DynaRub NDC 67777-113-50

Active Ingredient

Menthol 10%

Purpose

Topical Analgesic

Active Ingredient

Methyl Salicylate 15%

Purpose

Topical Analgesic

Uses

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

Warnings

For external use only

Do not use on

wounds or damaged skin

When using this product

avoid contact with eyes
do not bandage tightly

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

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: Consult a doctor

Other Information

store at 20°-25°C (68°-77°F).

Inactive Ingredients

Allantoin, Carbomer (Ultrez 10), Cetyl Alcohol, Dimethicone, Disodium EDTA, Glycerin, Glyceryl Monostearate, Isopropyl Myristate, Methyl Paraben, Phenoxyethanol, Potassium Cetyl Phosphate, Propyl Paraben, Purified Water, Sodium Hydroxide, Stearic Acid, Titanium Dioxide, Tween 20, Vitamin E, Xanthan Gum

Label

DYNARUB
pain relieving cream cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:67777-113
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (MENTHOL)	MENTHOL	10 g in 100 g
METHYL SALICYLATE (SALICYLIC ACID)	METHYL SALICYLATE	15 g in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALPHA-TOCOPHEROL ACETATE
XANTHAN GUM
POTASSIUM CETYL PHOSPHATE
PROPYLPARABEN
POLYSORBATE 20
GLYCERIN
GLYCERYL MONOSTEARATE
ISOPROPYL MYRISTATE
METHYLPARABEN
PHENOXYETHANOL
SODIUM HYDROXIDE
STEARIC ACID
EDETATE DISODIUM ANHYDROUS
WATER
ALLANTOIN
CARBOXYPOLYMETHYLENE
DIMETHICONE
CETYL ALCOHOL
TITANIUM DIOXIDE

Packaging
#	Item Code	Package Description
1	NDC:67777-113-50	72 TUBE in 1 CASE
1		85 g in 1 TUBE

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/12/2016

Labeler - Dynarex Corporation (008124539)

Document Id: 7f853941-a2d8-ed26-e053-2991aa0aa9ee

Set id: 7f853941-a2d7-ed26-e053-2991aa0aa9ee

Version: 1

Effective Time: 20190115

Dynarex Corporation

Further information

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

Medical Disclaimer