MIRACLE ICE description, usages, side effects, indications, overdosage, supplying and lots more!

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MIRACLE ICE

FDN Enterprises, LLC

MIRACLE ICE Arthritis Pain Reliever


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drug Facts

Active ingredient

Purpose

Active Ingredient Purpose
Menthol 1% Topical analgesic
Camphor 0.5% Topical analgesic

MIRACLE ICE 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

MIRACLE ICE 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

MIRACLE ICE

Menthol and Camphor (synthetic) GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:60691-114
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 1 g
CAMPHOR (SYNTHETIC) 0.5 g

Inactive Ingredients

Ingredient Name Strength
water
propylene glycol
methyl salicylate
SODIUM HYDROXIDE
METHYLPARABEN SODIUM
PROPYLPARABEN SODIUM
FD&C BLUE NO. 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:60691-114-30 227 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2013-07-15


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Be sure to consult your doctor before taking any medication!
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