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OLP PAIN-X

Medically reviewed on Nov 7, 2017

Dosage form: gel
Ingredients: MENTHOL, UNSPECIFIED FORM 25mg in 1g
Labeler: ohio lab pharma
NDC Code: 70648-005

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Active ingredient

Menthol 2.5%

Purpose

Topical analgesic

Uses

temporarily relieves the minor aches and pains of muscles and joints associated with:

  • simple backaches
  • arthritis
  • strains
  • bruises
  • sprains

Warnings

for external use only

Do not use
  • on wounds or damaged skin
  • with a heating pad
  • on a child under 12 years of age with arthritis-like conditions

Ask a doctor before use if you have redness over the affected area.

When using this product
  • avoid contact with eyes or mucous membranes
  • do not bandage tightly

Stop use and ask a doctor if
  • condition worsens or symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days
  • excessive skin irritation occurs

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center immediately.

Directions
  • adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
  • children under 12 years of age: ask a doctor

Other information
  • store at 20° to 25°C (68° to 77°F)

Inactive ingredients

Vitamin E, Propylene glycol,Polysorbate 80,Water, Isopropyl alcohol,Carbomer interpolymer typ A, edta, Methylparaben, Propylparaben.

Questions?

www.ohiolabpharma.us

Principal display panel 42.5 g tube carton

VANISHING SCENT
OLP PAIN-X
MENTHOL PAIN RELIEVING GEL

work on all types of minor arthritis pain

POWERFUL PAIN RELIEF FROM MINOR ARTHRITIS, BACKACHE, MUSCLE AND JOINT PAIN


NET WT. 1.5 OZ (42.5 g)

OLP PAIN-X 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:70648-005
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL, UNSPECIFIED FORM (MENTHOL, UNSPECIFIED FORM) MENTHOL, UNSPECIFIED FORM25 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
CARBOMER INTERPOLYMER TYPE A (55000 CPS) 
METHYLPARABEN 
PROPYLPARABEN 
.ALPHA.-TOCOPHEROL 
EDETATE DISODIUM 
POLYSORBATE 80 
ISOPROPYL ALCOHOL 
WATER 
PROPYLENE GLYCOL 
Packaging
#Item CodePackage Description
1NDC:70648-005-011 TUBE in 1 CARTON
142.5 g in 1 TUBE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34809/20/2016
Labeler - ohio lab pharma (080215854)
Registrant - OHIO LAB PHARMA (080215854)
Establishment
NameAddressID/FEIOperations
ohio lab pharma080215854manufacture(70648-005)

 
ohio lab pharma

Further information

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

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