SUMIFUN PAIN RELIEF CREAMS- methyl saliclate capsaicin camphor cream

Drug Labeling and Warnings

Drug Details [pdf]

ACTIVE INGREDIENT

Methyl Salicylate(10%)Capsaicin(0.025%).Camphor(5%)

PURPOSE

Uses
Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, ankle, back,
neck,hips, shoulders, elbows.

KEEP OUT OF REACH OF CHILDREN

OTC -KEEP OUT OF REACH OF CHILDRENCenter right away.
Keep out of reach of children. If swallowed, get medical help or contact a Poison Control

INACTIVE INGREDIENT

Inactive ingredients

Polyoxyl Stearate,Glyceryl Monostearate,Cetostearyl Alcohol,Purified Water,Phenoxyetha-nol,Edetate Calcium Disodium,Allantoin,Sodium Hydroxide,Carbomer 940,Dimethicone.

INDICATIONS & USAGE

DirectionsAdults and children 12 years of age and older:Rub a thin film over affected areas not more 4 times daily;Massage not necessaryChildren under 12 years of age:Consult physician;Wash hands after use with cool water.

DOSAGE & ADMINISTRATION

Rub a thin film over affected areas not more 4 times daily

WARNINGS

Warnings

For external use only.
Do not use

on wounds or damaged skinwith a heating pad or devicewith other ointments, creams, sprays,or linimentsif your are allergic to any ingredients of this product

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

SUMIFUN PAIN RELIEF CREAMS 
methyl saliclate capsaicin camphor cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87083-011
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR, (-)- (UNII: 213N3S8275) (CAMPHOR, (-)- - UNII:213N3S8275)	CAMPHOR, (-)-	5 g  in 100 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.025 g  in 100 g
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	10 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
ALLANTOIN (UNII: 344S277G0Z)
WATER (UNII: 059QF0KO0R)
EDETATE CALCIUM DISODIUM (UNII: 25IH6R4SGF)
PEG-120 STEARATE (UNII: 0V73PIX5YC)
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)
CARBOMER 940 (UNII: 4Q93RCW27E)
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)
DIMETHICONE (UNII: 92RU3N3Y1O)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
SODIUM HYDROXIDE (UNII: 55X04QC32I)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87083-011-01	30 g in 1 BOTTLE; Type 0: Not a Combination Product	04/12/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/12/2026

Labeler - Guchutang Biotechnology (Longyan) Co., Ltd (456645111)