Cryogel Island Rain Natural Pain Relieving description, usages, side effects, indications, overdosage, supplying and lots more!

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Cryogel Island Rain Natural Pain Relieving

Cosmetic Enterprises Ltd.
Cosmetic Enterprises Ltd.

Cryogel Natural Pain Relieving Gel Island Rain




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient                            Purpose

Menthol 3%                           Topical Analgesic

Purpose

Uses    Temporarily relieves the minor aches and pains of muscles and joints associated with

Strains

Sprains

Bruises

Simple Backache

Arthritis

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 immediately.

Uses

Stop use and consult a doctor if:

The condition worsens or persists for more than 7 days

Symptoms clear up and occur again within a few days

excessive skin irritation develops

Warning:

For external use only

Flammable keep away from excessive heat or open flame






















Inactive ingredients: water, alcohol, PEG-40 hydrogenated castor oil, ethoxydiglycol, propylene glycol, glycereth-26, MSM, Arnica Montana Ext, aloe, Camellia Ext, Hammamelis Ext, camphor, ascorbal palmitate, tocopheryl acetate, capsicuum annum, acrylates/C10-30 alkyl acrylate crosspolymer, methylparaben, disodium EDTA, metjylisothiazolinone, sodium hydroxide, fragrance, blue 1, yellow 5.

Cryogel Island Rain Natural Pain Relieving

Cryogel Island Rain Natural Pain Relieving Gel

Nt Wt: 4 oz. (114 gm)

Cryogel Island Rain Natural Pain Relieving

Cryogel Island Rain Natural Pain Relieving

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:56152-4006
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 3 g

Inactive Ingredients

Ingredient Name Strength
water
ISOPROPYL ALCOHOL
POLYOXYL 40 HYDROGENATED CASTOR OIL
propylene glycol
METHYLPARABEN
EDETATE DISODIUM
METHYLISOTHIAZOLINONE
SODIUM HYDROXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:56152-4006-1 114 in 1 TUBE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part346 2010-09-14


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Be sure to consult your doctor before taking any medication!
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