Relief by La Mend, Inc. RELIEF- menthol patch

Relief by

Drug Labeling and Warnings

Relief by is a Otc medication manufactured, distributed, or labeled by La Mend, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol (plant derived) 5%

PURPOSE

Topical Analgesic

INDICATIONS & USAGE

WARNINGS

For external use only

WHEN USING

• use only as directed
• avoid contact with the eyes and other mucous membranes
• do not apply to wounds or damaged skin
• do not bandage tightly
• use only as directed

DO NOT USE

• more than one patch at a time
• at the same time as other topical analgesics

STOP USE

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

PREGNANCY OR BREAST FEEDING

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 Posion Control Center right away.

DOSAGE & ADMINISTRATION

adults over 18 years:

• use one patch
• carefully remove the backing film and apply to the affected area no more than 3 to 4 times daily
• each patch can be worn up to 12 hours
• children under 18 years of age: consult a doctor

STORAGE AND HANDLING

• store in a cool, dry place

INACTIVE INGREDIENT

methyl acrylate, 2-ethylhexyl acrylate, acrylic acid copolymer, hydroxyethyl acrylate, vinyl acetate copolymer, lavender oil, arnica montana extract, aloe vera extract, eucalyptus oil

QUESTIONS

(310) 909-8407 | thegoodpatch.com

You may also report serious side effects to this phone number

PRINCIPAL DISPLAY PANEL

Relief

QTY. 04 PATCHES

Pain holding you back? Keep moving with this fast-acting, water-resistant topical patch. Made with plant-derived Menthol, Lavender, Arnica, and Aloe Vera.

INGREDIENTS AND APPEARANCE

RELIEF 
menthol patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72587-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72587-002-01	1 in 1 BOX	04/15/2022	05/01/2025
1		1 in 1 POUCH
1		1.35 g in 1 PATCH; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/15/2022	05/01/2025

Labeler - La Mend, Inc. (117940830)