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

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Calypxo Pain Relief

Enovachem Manufacturing


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

Drugs Facts

Active Ingredients

Methyl Salicylate……….10.00%

Menthol…………………...3.00%

Purpose

Topical Analgesic

Topical Analgesic

Uses

For temporary relief of minor aches and pains associated with simple backaches, arthritis, bruises, sprains and cramps.

Warning

For external use only.

Avoid contact with eyes and mucous membranes.

Do not bandage tightly or cover treated areas.

Do not use with heating pad.

Do not apply to open wounds or damages skin.

A mild burning sensation may occur. If severe burning sensation occurs, discontinue use immediately.

If symptoms persist for more than seven days, discontinue use and consult physician.

Keep out of reach of children. If swallowed, consult physician.

If pregnant or breast feeding, contact physician prior to use.

Directions

For adults apply directly to effected area. Repeat as necessary, but do not use more than 3-4 times daily.

Other Ingredients

Acrylates/C10-30 Alkyl Acrylate Crosspolymer, Aloe Barbadensis Leaf (Aloe Vera Gel) Juice, Aqua (Deionized Water), Cetyl Alcohol, Diazolidinyl Urea, Isopropyl Myristate, Methyl Paraben, PEG-8, Propyl Paraben, Propylene Glycol, Sodium lauryl Sulfate, Triethanolamine.

Principal Display Panel – Front Label

NDC 76420-0450-12

Calypxo

Pain Relief Cream

4 OZ (113g)

Distributed by:

Enovachem Manufacturing

Torrance, CA 90501

(310) 218-4146

Calypxo Pain Relief

Methyl Salicylate, Menthol CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:76420-450
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
methyl salicylate METHYL SALICYLATE 10 g
MENTHOL 3 g

Inactive Ingredients

Ingredient Name Strength
CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED)
Aloe Vera Leaf
water
CETYL ALCOHOL
DIAZOLIDINYL UREA
ISOPROPYL MYRISTATE
METHYLPARABEN
polyethylene glycol 400
PROPYLPARABEN
propylene glycol
SODIUM LAURYL SULFATE
TROLAMINE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:76420-450-12 113 in 1 BOTTLE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2014-01-15


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Be sure to consult your doctor before taking any medication!
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