MEDI-FIRST PAIN RELIEF- analgesic- menthol spray

Medi-First Pain Relief by

Drug Labeling and Warnings

Medi-First Pain Relief by is a Otc medication manufactured, distributed, or labeled by Unifirst First Aid Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient

USP Menthol 7%

Purpose

Topical analgesic

Uses

Temporary relief of minor aches and pains of muscles and joints.

Warnings

For external use only. Flammable. Keep away from flame.

Do not use

• on open wounds or damaged skin

Asl a doctor before use if

• you are prone to allergic reactions to salicylates, including aspirin

When using this product

• avoid contact with the eyes

Stop use and ask a doctor if

• condition worsens
• symptoms persist for more than 7 days or clear upand recur again within a few days
• excessive skin irritation occurs

If pregnant or breast feeding,

ask a doctor before use.

Keep out of reach of children.

If swallowed, grt medical help or contact a Poison Control Center right away.

Directions

Adults and children (2 years and older):

Shake well and apply to affected area not more than 3-4 times daily.

Do not bandage tightly.

Children under 2 years:

consult a doctor.

Other information

• store at room temperature 59°- 86°F (15°- 30”C)
• will not stain clothing

Inactive ingredients

coconut oil, eucalyptus leaf oil, glycerol, isopropyl alcohol, peppermin oil, water, wintergreen leaf oil

Questions or comments?

1-800-634-7680

Medi-First Pain Relief Spray Label

Medi-First®

Pain Relief Spray

Pump Spray

Medicated Fast Acting

For the temporary relief of minor aches and pains

2 FL OZ (59.1 mL)

INGREDIENTS AND APPEARANCE

MEDI-FIRST PAIN RELIEF 
analgesic- menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 47682-235
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	70 mg  in 1 L

Inactive Ingredients
Ingredient Name	Strength
ISOPROPYL ALCOHOL (UNII: ND2M416302)
EUCALYPTUS OIL (UNII: 2R04ONI662)
METHYL SALICYLATE (UNII: LAV5U5022Y)
COCONUT OIL (UNII: Q9L0O73W7L)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
PEPPERMINT OIL (UNII: AV092KU4JH)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 47682-235-02	0.059 L in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	04/01/2019

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph not final	part348	04/01/2019

Labeler - Unifirst First Aid Corporation (832947092)

Establishment
Name	Address	ID/FEI	Business Operations
Prestige Packaging		170837962	relabel(47682-235) , repack(47682-235)