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Antiphlamine Pain Relieving

Medically reviewed by Drugs.com. Last updated on Oct 4, 2021.

Dosage form: patch
Ingredients: Flurbiprofen 33mg
Labeler: HANUL TRADING CO., LTD.
NDC Code: 69642-1300

ACTIVE INGREDIENT

Active Ingredient: Flurbiprofen 33mg

INACTIVE INGREDIENT

Inactive Ingredients: Methylparaben, Propylparaben, L-menthol, Propylene Glycol, Glycerin, Titanium Oxide, Kaolin, Sodium Carboxymethyl Cellulose, Dihydroxyaluminum Aminoacetate Hydrate, Disodium Edetate Hydrate, Gelatin, Sodium Polyacrylate, Polyacrylic Acid solution, Ferric Oxide, Butylhydroxytoluene, Purified water, felt, attachment felt, Polyethyleneterephthalate Separator, propyleneglycol monocaprylate, Sorbitan Oleate, tartaric acid

PURPOSE

Purpose: Topical Analgesic

WARNINGS

Warnings: For external use only Ask a doctor before use if you have redness over the affected area. Do not use: on wounds or damaged skin. Stop use and ask a doctor if excessive skin irritation occurs. Do not use if you are pregnant or breast feading. Do not use if you are allergic to any of the ingredients(Aspirin, Flurbiprofen) and stop use if rash, itching or allergic reaction develops.

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children: Keep out of reach of children to avoid accidental ingestion. If swallowed, get medical help or contact a Poison Control Center immediately. Children under 12 years of age: Ask a doctor Children under 30 month: Do not use

INDICATIONS & USAGE

Indications & Usage: For the temporary relief of Shoulder Pain, Backache, Neuralgia, Arthralgia, Sore Muscles, Sprains, Bruises, Rheumatic Pain, and Fracture Pain.

DOSAGE & ADMINISTRATION

Dosage & Administration: Attach to the affected part, twice daily

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ANTIPHLAMINE PAIN RELIEVING 
flurbiprofen patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69642-1300
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Flurbiprofen (FLURBIPROFEN) Flurbiprofen33 mg  in 5 
Inactive Ingredients
Ingredient NameStrength
Methylparaben 
Propylparaben 
Packaging
#Item CodePackage Description
1NDC:69642-1300-15 PATCH in 1 CELLO PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other09/01/2015
Labeler - HANUL TRADING CO., LTD. (689512982)
Registrant - HANUL TRADING CO., LTD. (689512982)
Establishment
NameAddressID/FEIOperations
HANUL TRADING CO., LTD.689512982repack(69642-1300)
Establishment
NameAddressID/FEIOperations
Dae Hwa Pharm Co., Ltd.688004324manufacture(69642-1300)
Establishment
NameAddressID/FEIOperations
KOCO TRADING CO., INC.079457993wholesale drug distributor(69642-1300)

 
HANUL TRADING CO., LTD.

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.