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

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Mini Pain Relief

Shanghai Aquagel Bio-Plymer Co., Ltd

Drug Facts




FULL PRESCRIBING INFORMATION

Inactive ingredients Ammonium Stearate, Calcium Carbonate, Glyceryl Abietate, Isopropyl Myristate, Natural
Rubber,Polybutene, Polyisobutylene, Propylene Carbonate, Styrene Copolymer, YS Resin, Zinc Oxide

Active ingredient

Active ingredients

DL-Camphor 1.2%

L-Menthol 2,.%

Methyl Salicylate 2.5%

Purpose

Purpose

Topical Analgesic

Keep out of reach of children. If swallowed, get medical help or contact a poison control center immediately

Uses

Do not use

other than as directed on wounds, damaged or irritated skin in combination with other
external analgesic products, ointments, creams or with a heating pad. in contact with eyes or mucous
membranes. if you are allergic to any ingredient in this product or if you have a history of allergic reactions to this
or similar products

Stop Use and ask a
doctor if


rash, itching or excessive skin irritation develops

condition worsens

symptoms persist for more
than 7 days

if symptoms
subside and then reappear within a few days.

Warnings

For External Use Only

Directions

Adults and children 12 years of age and over: Clean and dry the affected area. Remove
patch from film backing. Adhere to area for no more than 8 hours at a time, not more than 3 times per day, and for no more
than 7 days continuously. Children under 12 years of age: Consult a doctor before use.

Uses

For temporary relief of minor aches and pains associated with:

Arthritis

Backaches

Sprains

Strains

Bruises

Mini Pain Relief

Mini Pain Relief

DL-Camphor L-Menthol Methyl Salicylate PATCH

Product Information

Product Type Human otc drug label Item Code (Source) NDC:53043-003
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
CAMPHOR (SYNTHETIC) 1.2 mg
LEVOMENTHOL 2.7 mg
methyl salicylate METHYL SALICYLATE 2.5 mg

Inactive Ingredients

Ingredient Name Strength
AMMONIUM STEARATE
CALCIUM CARBONATE
GLYCERYL ABIETATE
ISOPROPYL MYRISTATE
NATURAL LATEX RUBBER
POLYBUTENE (1400 MW)
Polyisobutylene (1000 MW)
PROPYLENE CARBONATE
STYRENE
Zinc Oxide

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:53043-003-01 20 in 1 CARTON
2 NDC:53043-003-02 20 in 1 CARTON

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
part part348 2012-12-01


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