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Miracle Ice Ultra Strength

Dosage form
GEL
Labeler
FDN Enterprises,LLC
Label updated
2013-09-20
Retrieved
2026-09-07
Active ingredients
Camphor (synthetic) · Menthol
View original label and images on DailyMed ↗
Label information

Drug Facts

유효 성분

성분·작용

Active Ingredient Purpose
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

Label information

Do not use

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

Label information

When using this product

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

Label information

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

Label information

If pregnant or breast-feeding, ask a health professional before use.

Label information

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, CI 14720, CI 16185, CI 42090

Label information

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

PRINCIPAL DISPLAY PANEL - 227 g Jar Label

FDN Medical ®
MIRACLE
ICE

ULTRA STRENGTH

ANALGESIC GEL

NET WT. 8 OZ (227 g)

[Image in the official label — see DailyMed source]

DailyMed Set ID: ae7dcb00-f53b-4c96-84bc-7c21ea427592 · Version 1
NDC: 60691-116