Sofskin Ice Analgesic description, usages, side effects, indications, overdosage, supplying and lots more!

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Sofskin Ice Analgesic

Nova Petroleum & Chemicals Corporation

Ice Analgesic Gel




FULL PRESCRIBING INFORMATION

Label for

NOVA PETROLEUM & CHEMICALS CORP.

Ice Analgesic Gel

Drug Facts:

Menthol 1%

Topical Analgesic

Provide temporary relief of minor aches and pains in muscles and joints associated with samples backache, strains, sprains, arthritis sports injuries.

For external use only-Not for internal use.

Use only as directed. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged skin. Make sure skin is clean and free from any creams, ointments, sprays or liniment. Do not bandage.

with heating pads or heating devices.

If condition worsens or symptoms persist for more than 7 days or if symptoms disappear and occur again within a few days, discontinue use and consult a physician. If you have sensitive skin, consult a physician before use. If skin irritation develops, discontinue use and consult a physician. If you are pregnant or nursing a baby consults your doctor before use. Do not use, store, pour or spill near heat or open flames. Store in a cool, dry place and keep lid tightly closed.

Clean skin of all other lotions, creams, ointments, liniment or sprays, Apply liberally to affected area and massage until gel is absorbed into skin. Do not apply more than 3 or 4 times daily. No protective cover needed. Do not apply to children under 2 years of age.

            Made in India

Imported by:

      Nova Petroleum & Chemicals Corp.

      3 Roethal Drive Suite 1 D

      Hopewell Junction, NY 12533

      www.novawax.com

Distributed by: 

      Vini Health and Beauty Products Inc.

      3 Roethal Drive Suite 1 D

      Hopewell Junction, NY 12533

Sofskin
Ice analgesic gel
Fast, temporary relief from muscle aches and pains
Net Wt. 7 Oz. (200 g)

Sofskin Ice Analgesic

Sofskin Ice Analgesic

Menthol GEL

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52069-104
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 2.27 g

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52069-104-07 227 in 1 JAR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part341 2010-03-10


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