Pain Relieving Patch description, usages, side effects, indications, overdosage, supplying and lots more!

Menu
Search

Pain Relieving Patch

Heilongjiang Huashen Science & Technology Development Co Ltd
Heilongjiang Huashen Science & Technology Development Co Ltd

Pain Relieving Patch




FULL PRESCRIBING INFORMATION

Active ingredient

Active Ingredient ( in each patch)               Purpose

Menthol 0.2 percent                                       Analgesic

Purpose




Warnings:

For external use only. Avoid contact with the eyes.

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again

within a few days, discontinue use of this product and consult a doctor.



Do not use

- otherwise than as directed

- in the eyes or ears

- if you are pregnant

- if you have skin allergy or damage to skin

Stop use and ask a doctor if

- redness is present

- excessive irritation of the skin develops

- side effects occur. You may report side effects to FDA at 1-800-FDA-1088

Keep  out of reach of children.

Directions:

Adults and children 2 years of age and older:  Remove patch from package. Apply to affected area not more than 3-4 times daily. Leave bandage

                                                                                  on for no more than 48 hours.



Children under 2 years of age: Consult a doctor.

Manufactured by:

Heilongjiang Huashen Science and Technology

Development Co. Ltd. China

Investment Building, No.235 HongQi Street,

High and New Technology Development Zone,

Harbin, HeilLongjiang Province, China

86 451 82262828

hs huashen.net

www.huashen.net


Product of China

Distributed By:

Exclusive Representation Center of

Huashen Corporation

1635 Bath Ave

Brooklyn, NY 11214

718 841 7770

HuaShen Pain Relieving Patch

Continuous Relief for up to

48

hours

- fast

- effective

- natural

5 Adhesive Patches with Menthol

Pain Relieving Patch

Pain Relieving Patch

MENTHOL PATCH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:50309-777
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MENTHOL 0.2 1

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:50309-777-15 5 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2010-01-30


PLEASE, BE CAREFUL!
Be sure to consult your doctor before taking any medication!
Copyright © 2014. drugs-library.com. All rights reserved. Information on drugs-library.com is provided for educational purposes only and is not to be used for medical advice, diagnosis or treatment.
Support info@drugs-library.com.