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MIRACLE ICE Arthritis Pain Reliever

Dosage form: gel
Ingredients: Menthol 1g in 100g, Camphor (synthetic) 0.5g in 100g
Labeler: FDN Enterprises, LLC
NDC code: 60691-114

Medically reviewed by Drugs.com. Last updated on Sep 10, 2024.

MIRACLE ICE
Arthritis Pain Reliever

Drug Facts

Active IngredientPurpose
Menthol 1%Topical analgesic
Camphor 0.5%Topical analgesic

Uses
  • temporarily relieves minor aches and pains of muscles and joints associated with:
    • arthritis
    • simple backache
    • strains
    • bruises
    • sport injuries
    • sprains

Warnings

For external use only

Do not use

  • with other topical pain relievers
  • with heating pads or heating devices

When using this product

  • do not use in or near the eyes
  • do not apply to wounds or damaged skin
  • do not bandage tightly

Stop use and ask a doctor if

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

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 Poison Control Center right away.

Directions
  • clean affected area before applying product
  • adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily.
  • children under 2 years of age: ask a doctor

Other information
  • Store at room temperature 59°-86°F (15°-30°C).
  • Keep jar tightly closed and away from open heat or flame

Inactive ingredients

Aqua, Propylene Glycol, Carbomer, Methyl Salicylate, Sodium Hydroxide, Sodium Methyl Paraben, Sodium Propyle Paraben, FD&C Blue#1, CI 42090.

Distributed by:
FDN Enterprises, LLC.
Opa Locka, FL 33054

PRINCIPAL DISPLAY PANEL - 227 g Jar Label

FDN Medical®

MIRACLE
ICE

ARTHRITIS PAIN RELIEVER

ANALGESIC GEL

NET WT. 8 OZ (227 g)

MIRACLE ICE   ARTHRITIS PAIN RELIEVER
menthol and camphor (synthetic) gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:60691-114
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Menthol (Menthol) Menthol1 g  in 100 g
Camphor (synthetic) (Camphor (synthetic)) Camphor (synthetic)0.5 g  in 100 g
Inactive Ingredients
Ingredient NameStrength
Water 
Propylene Glycol 
Methyl Salicylate 
Sodium Hydroxide 
METHYLPARABEN SODIUM 
PROPYLPARABEN SODIUM 
FD&C BLUE NO. 1 
Packaging
#Item CodePackage Description
1NDC:60691-114-30227 g in 1 JAR
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart34807/15/2013
Labeler - FDN Enterprises, LLC (965743867)

Revised: 09/2013
Document Id: 92907e2a-bd56-4f22-91c7-801f26ca4905
Set id: 1112a854-1238-44ef-b5a0-d19cbfa89c5a
Version: 1
Effective Time: 20130920
 
FDN Enterprises, LLC

Further information

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

Medical Disclaimer