OTC Medication Information: Pain Relief

PAIN RELIEF- menthol spray
Unifirst First Aid Corporation

Drug Facts

Active ingredients

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

Ask a doctor before use if

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

When using this product

  • avoid contact with eyes

Stop use and ask a doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and 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, get medical help or contact a Poison Control Center right away.

Directions

Adults and children (2 years and older):

Shake well and aply to affected araea not more than 3-4 times daily.

Do not bandage tightly.

Children under 2 years:

Consult a doctor

Other information

  • store at room temperature 56°-86°F (15°-30°C)
  • will not stain clothing

Inactive ingredients

coconut oil, eucalyptus lkeaf oil, glycerol, isopropyl alcohol, peppermint oil, water, wintergreen leaf oil

Questions or comments?

1-800-869-6970

Green Guard Pain Relief Spray Label

Pain Relief spray

Fast Acting pain Relief

For Temporary Relief of Minor Aches and Pains

Green Guard®

2 Fl. Oz. (59.1 mL)

Green Guard
(click image for full-size original)
PAIN RELIEF
analgesic menthol spray
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:47682-321
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (MENTHOL) MENTHOL 70 mg in 1 L
Inactive Ingredients
Ingredient Name Strength
COCONUT OIL
ISOPROPYL ALCOHOL
EUCALYPTUS OIL
GLYCERIN
WATER
METHYL SALICYLATE
PEPPERMINT OIL (PEPPERMINT)
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:47682-321-02 0.059 L in 1 BOTTLE, SPRAY None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M015 04/01/2019
Labeler — Unifirst First Aid Corporation (832947092)

Revised: 01/2024 Unifirst First Aid Corporation

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Terms of Use | Copyright © 2024. All Rights Reserved.