MINI PAIN RELIEF- dl-camphor l-menthol methyl salicylate patch

Mini Pain Relief by

Drug Labeling and Warnings

Mini Pain Relief by is a Otc medication manufactured, distributed, or labeled by Shanghai Aquagel Bio-Plymer Co., Ltd. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

INACTIVE INGREDIENT

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

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

INDICATIONS & USAGE

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

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

Warnings

For External Use Only

DOSAGE & ADMINISTRATION

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.

INSTRUCTIONS FOR USE

Uses

For temporary relief of minor aches and pains associated with:

Arthritis

Backaches

Sprains

Strains

Bruises

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

MINI PAIN RELIEF 
dl-camphor l-menthol methyl salicylate patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 53043-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	1.2 mg
LEVOMENTHOL (UNII: BZ1R15MTK7) (LEVOMENTHOL - UNII:BZ1R15MTK7)	LEVOMENTHOL	2.7 mg
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	2.5 mg

Inactive Ingredients
Ingredient Name	Strength
AMMONIUM STEARATE (UNII: 37899330TZ)
CALCIUM CARBONATE (UNII: H0G9379FGK)
GLYCERYL ABIETATE (UNII: 2F22LY70Q1)
ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS)
NATURAL LATEX RUBBER (UNII: 2LQ0UUW8IN)
POLYBUTENE (1400 MW) (UNII: 1NA5AO9GH7)
POLYISOBUTYLENE (1000 MW) (UNII: 5XB3A63Y52)
PROPYLENE CARBONATE (UNII: 8D08K3S51E)
STYRENE (UNII: 44LJ2U959V)
ZINC OXIDE (UNII: SOI2LOH54Z)

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
OTC monograph not final	part348	12/01/2012

Labeler - Shanghai Aquagel Bio-Plymer Co., Ltd (421199544)

Establishment
Name	Address	ID/FEI	Business Operations
Shanghai Aquagel Bio-Plymer Co., Ltd		421199544	manufacture(53043-003, 53043-003)