ASSURED MENTHOL RELIEF STICK- menthol stick

Assured Menthol Relief Stick by

Drug Labeling and Warnings

Assured Menthol Relief Stick by is a Otc medication manufactured, distributed, or labeled by VVF Kansas Services LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Menthol 2 %

Purpose

Topical analgesic

Uses

Temporarily relieves minor aches and pains associated with:

• arthritis
• simple backaches
• muscle strains
• muscle sprains
• bruises
• cramps

Warnings

For external use only.

If pregnant or breast-feeding, ask a health professional before use.

Allergy Alert: Do not use if allergic to salicylates (including aspirin) without consulting a physician.

When using this product

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

Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days or clear up and occur again within a few days
• redness is present
• irritation develops

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 or older

• Apply generously to affected area
• Massage into area until thoroughly absorbed into skin
• Repeat as necessary, but no more than 4 times daily

Children under 12 years of age: consult a doctor

Inactive ingredients

Propylene Glycol, Water, Sodium Stearate, Methyl Salicylate, Stearamide MEA, PEG-150 Distearate, Hydrogenated Castor Oil.

Questions or comments?

1-800-323-5385

SPL UNCLASSIFIED SECTION

MADE IN U.S.A.

DISTRIBUTED BY GREENBRIER INTERNATIONAL, INC.

500 VOLVO PARKWAY CHESAPEAKE, VA 23320

UPC: 639277689412

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

ASSURED MENTHOL RELIEF STICK 
menthol stick

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10889-203
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.34 g  in 57 g

Inactive Ingredients
Ingredient Name	Strength
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM STEARATE (UNII: QU7E2XA9TG)
METHYL SALICYLATE (UNII: LAV5U5022Y)
PEG-150 DISTEARATE (UNII: 6F36Q0I0AC)
HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)
STEARAMIDE (UNII: YQX129FH1U)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10889-203-01	57 g in 1 APPLICATOR; Type 0: Not a Combination Product	09/01/2013

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	09/01/2013	05/01/2020

Labeler - VVF Kansas Services LLC (833164242)

Registrant - VVF Kansas Services LLC (833164242)

Establishment
Name	Address	ID/FEI	Business Operations
VVF Kansas Services LLC		833164242	manufacture(10889-203)