EQUALINE BLUE ICE PAIN RELIEVING description, usages, side effects, indications, overdosage, supplying and lots more!

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EQUALINE BLUE ICE PAIN RELIEVING

Supervalu Inc

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                                                                       Purpose

Menthol 2.0% ..........................................................................Topical Analgesic

Purpose

Uses: Temporary relief of minor aches and pains in: Muscles and joints.

Warnings:

For external use only.  Avoid contact with eyes and mucus membranes.

When using this product do not:

  • 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

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.

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

Uses

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 skin. Repeat no more than 3-4 times daily

Inactive Ingredients: Aqua (water), Isopropyl Alcohol, Carbomer, Thymol, Ammonium Hydroxide, Sodium Hydroxide, Magnesium Sulfate, FD and C Blue No.1

DISTRIBUTED BY SUPERVALU INC.

EDEN PRAIRIE, MN 55344 USA

MADE IN CANADA

EQUALINE BLUE ICE PAIN RELIEVINGEnter section text here

EQUALINE BLUE ICE PAIN RELIEVING

MENTHOL GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:41163-488
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 2 g

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL ALCOHOL
THYMOL
AMMONIA
SODIUM HYDROXIDE
MAGNESIUM SULFATE, UNSPECIFIED

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:41163-488-32 227 in 1 CONTAINER

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-10-03


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