Blue Ice Analgesic description, usages, side effects, indications, overdosage, supplying and lots more!

Blue Ice Analgesic

Delon Laboratories (1990) Ltd

  • Description
  • Clinical Pharmacology
  • Indications & Usage
  • Contraindications
  • Warnings
  • Precautions
  • Side Effects
  • Overdosage
  • Dosage & Administration
  • How Supplied
  • Patient Counseling Information
  • Supplemental Patient Material
  • Boxed Warning
  • Patient Package Insert
Drug Facts

FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient / Purpose



Uses



  • muscles and joints

Directions

  • Put a small amount onto your palms and rub hands together until dry.

Warnings

  • For external use only. Avoid contact with eyes and mucous membranes.





  • use with heating pads or heating devices
  • use, pour, spill, or store near open flame
  • use with other creams, sprays or liniments
  • apply to damaged skin or wounds - Bandage area tightly


  • Keep out of reach of children. In case of accidental ingestion, get medical help or contact a Poison Control Center right away.

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician. If you have sensitive skin consult a physician. If skin irritation develops, discontinue use and seek the advice of a physician before using this product.

Directions

  • See important warnings under when using this product
  • Do not apply to children under 2 years of age, unless advised by a physician.
  • Adults and children over 2 years and older: Apply liberally to painful area and massage until gel is absorbed into the skin. Repeat 3 to 4 times daily.

Inactive Ingredients

Deinoized Water, Isopropyl Alcohol, Carbomer, Thymol, Ammonium Hydroxide, Sodium Hydroxide, Magnesium sulfate, FDC Blue 1

mm1


Blue Ice Analgesic

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:61734-021
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 2.0 g

Product Characteristics

Color
blue

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:61734-021-01 100 in 1 BOTTLE, PUMP
2 NDC:61734-021-02 113.56 in 1 CONTAINER
3 NDC:61734-021-03 227 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2010-05-07


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