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EQUALINE BLUE ICE PAIN RELIEVING

Dosage form
GEL
Labeler
SUPERVALU INC
Label updated
2011-10-03
Retrieved
2026-09-07
Active ingredients
MENTHOL
View original label and images on DailyMed ↗
유효 성분

Active Ingredient                                                                       Purpose

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

성분·작용

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

주의사항

Warnings:

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

Label information

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
To do so may result in excessive skin irritation or skin burn.
Label information

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.

Label information

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

효능·용도

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
첨가제

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

복용법·사용법

DISTRIBUTED BY SUPERVALU INC.

EDEN PRAIRIE, MN 55344 USA

MADE IN CANADA

포장 표시

[Image in the official label — see DailyMed source]

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DailyMed Set ID: 7a652b7c-662d-4605-814d-86cf5084797f · Version 1
NDC: 41163-488