Otc - Active Ingredient
Methyl Salicylate(10%)Capsaicin(0.025%).Camphor(5%)
Sumifun Pain Relief Creams Cream
FDA Label NDC 87083-011
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guchutang Biotechnology (longyan) Co., Ltd for the product Sumifun Pain Relief Creams (NDC 87083-011). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding otc - active ingredient, otc - purpose, otc - keep out of reach of children, inactive ingredient, indications & usage, dosage & administration, warnings, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses
Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, ankle, back,
neck,hips, shoulders, elbows.
Otc - 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
Package Label.Principal Display Panel
Labeling (87083 011 01)
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