Coralite Pain Relief description, usages, side effects, indications, overdosage, supplying and lots more!

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Coralite Pain Relief

UNITED EXCHANGE CORP.


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Coralite Pain Relief Patch 20 Ct

Active ingredients                                     Purpose

DL-Camphor 1.2%.................................. Topical Analgesic

L-Menthol 5.7%...................................... Topical Analgesic

Methyl Salicylate 6.3%............................ Topical Analgesic

Purpose

Uses

For temporary relief of minor aches and pains of muscles and joints associated with:

  • arthritis
  • simple backache
  • strains
  • bruises
  • sprains

Warnings

For external use only

Do not use

  • on wounds or damaged skin
  • if you are allergic to aspirin or salicylates
  • with a heating pad
  • with, or at the same time as, other external analgesic products

Ask a doctor before use if you allergic to any ingredients of this product

When using this product

  • do not use other than directed
  • avoid contact with the eyes, mucous membranes or rashes

Stop use and ask a doctor if

  • rash, itching or excessive skin irritation develops
  • conditions worsen symptoms persist for more than 7 days
  • symptoms clear up and occur again within a few days

Keep out of reach of children. If swallowed, get medical help or conduct a Poision Control Center right away

Caution: This product contains natural rubber latex which may cause allergic reactions

Uses

Other information

  • avoid storing product in direct sunlight
  • protect from excessive moisture

Inactive ingredients BHT, calcium carbonate, C4-6 olefin/styrene copolymer, glyceryl abiertate, isopropyl myristate, polybutene, polyisobutylene, propylene carbonaterubber latex, sorbitan stearate, ys resin, zinc oxide

DISTRIBUTED BY:

UNITED EXCHANGE CORP.

17211 VALLEY VIEW AVE.

CERRITOS, CA 90703 USA

Coralite Pain Relief

Coralite Pain Relief

DL-Camphor, L-Menthol, Methylsalicylate PATCH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:65923-156
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAMPHOR (SYNTHETIC) 1.2 g
LEVOMENTHOL 5.7 g
methyl salicylate METHYL SALICYLATE 6.3 g

Inactive Ingredients

Ingredient Name Strength
BUTYLATED HYDROXYTOLUENE
CALCIUM CARBONATE
STYRENE
GLYCERYL ABIETATE
ISOPROPYL MYRISTATE
Polyisobutylene (1000 MW)
POLYBUTENE (1400 MW)
PROPYLENE CARBONATE
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 1 in 1 PATCH
2 NDC:65923-156-20 20 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-03-26


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
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