EFAC Pain Relieving

Dosage form: cream
Ingredients: MENTHOL, UNSPECIFIED FORM 12.5mg in 1g
Labeler: Hope Science Inc.
NDC code: 71970-302

Medically reviewed by Drugs.com. Last updated on Mar 18, 2024.

EFAC
Pain Relieving Cream

Drug Facts

Active Ingredients

Menthol (1.25%)

Purpose

Topical Analgesic

Indications

For 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.
Avoid contact with eyes.
If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of product and consult a physician.
Do not apply to wounds or damaged skin.
Do not bandage tightly.

Keep out of reach of children.
If swallowed, get medical help or contact a poison control center right away.

Directions

Adults and children 2 yrs. of age and older, apply to affected area not more than 3 to 4 times a day. Children under 2 yrs. of age, consult a physician.

Other Information

Store in a cool, dry place.

Inactive Ingredients

Benzyl Alcohol, Butylparaben, Carbomer, Esterified Fatty Acids (Proprietary Blend), Ethylparaben, Glycerin, Glyceryl Stearate, Isobutylparaben, Lecithin, Methylparaben, Olea Europaea (Olive) Fruit Oil, PEG-100 Stearate, Peppermint Oil, Phenoxyethanol, Potassium Hydroxide, Propylparaben, Tocopheryl Acetate, Water.

Questions?

1-866-628-8725
www.HopeScience.com

Distributed by Hope Science Inc.

PRINCIPAL DISPLAY PANEL - 16 oz. Bottle Label

FEEL the Difference!

Clinically Tested MORE Effective

EFAC

PAIN Relieving Cream
TOPICAL ANALGESIC

16 oz.

Maximum Absorption!

EFAC PAIN RELIEVING
menthol, unspecified form cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:71970-302
Route of Administration	TOPICAL	DEA Schedule

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL, UNSPECIFIED FORM (MENTHOL, UNSPECIFIED FORM)	MENTHOL, UNSPECIFIED FORM	12.5 mg in 1 g

Inactive Ingredients
Ingredient Name	Strength
BENZYL ALCOHOL
BUTYLPARABEN
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
CETYL TALLOWATE
ETHYLPARABEN
GLYCERIN
GLYCERYL MONOSTEARATE
ISOBUTYLPARABEN
LECITHIN, SOYBEAN
METHYLPARABEN
OLIVE OIL
PEG-100 STEARATE
PEPPERMINT OIL
PHENOXYETHANOL
SODIUM HYDROXIDE
PROPYLPARABEN
.ALPHA.-TOCOPHEROL ACETATE
WATER

Product Characteristics
Color	WHITE	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description
1	NDC:71970-302-45	113 g in 1 JAR
2	NDC:71970-302-49	454 g in 1 BOTTLE, PLASTIC

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC MONOGRAPH NOT FINAL	part348	10/01/2012

Labeler - Hope Science Inc. (049917199)

Registrant - Lifetech Resources LLC (622559110)

Establishment
Name	Address	ID/FEI	Operations
Lifetech Resources LLC		622559110	MANUFACTURE(71970-302)

Document Id: 5ab2658e-eee3-4221-a209-ca4ebbfd0486

Set id: 781ae47d-91c5-4b36-8b53-f8b895efe9c5

Version: 1

Effective Time: 20180326

Hope Science Inc.

Further information

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

Medical Disclaimer

Migraine 101