QC Cold and Hot Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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QC Cold and Hot Pain Relief

CHAIN DRUG MARKETING ASSOCIATION INC

Drug Facts


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Active Ingredient


Purpose

Topical Analgesic

QC Cold and Hot Pain Relief Uses

temporarily relieves minor pain associated with

  • arthritis
  • simple backache
  • bursitis
  • tendonitis
  • muscle strains
  • sprains
  • bruises
  • cramps

Warnings

For external use only

When using this product

  • use only as directed
  • avoid contact with eyes and mucous membranes
  • do not bandage tightly or use with a heating pad
  • do not apply to wounds or damaged skin, broken or irritated skin

Stop use and ask a doctor if

  • condition worsens
  • redness is present
  • irritation develops
  • symptoms persist for more than 7 days or clear up and occur again within a few days

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

Adults and children over 12 years:

  • carefully remove backing from patch
  • apply one patch to affected area
  • repeat as necessary, but no more than 4 times daily

Children 12 years or younger: ask a doctor

Inactive ingredients

Acrylic Acid, Aluminum Hydroxide, Carmellose sodium, 2-Ethylhexyl Acrylate, Glycerin, Isopropyl Myristate, Methyl Acrylate, Nonoxymol-30, Sodium Polyacrylate, Polyacrylic Acid, Polysorbate 80, Purified Water, Sorbitan Sesquioleate, Starch, Talc, Tartaric acid, Titanium Dioxide

package label

QC Cold and Hot PatchQC Cold and Hot Pain Relief

QC Cold and Hot Pain Relief

Menthol PATCH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:63868-012
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 400 mg

Inactive Ingredients

Ingredient Name Strength
ACRYLIC ACID
aluminum hydroxide
CARBOXYMETHYLCELLULOSE SODIUM
GLYCERIN
ISOPROPYL MYRISTATE
METHYL ACRYLATE
NONOXYNOL-30
polysorbate 80
SORBITAN SESQUIOLEATE
talc
tartaric acid
titanium dioxide
water

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 5 in 1 POUCH
2 NDC:63868-012-05 1 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2011-09-12


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Be sure to consult your doctor before taking any medication!
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