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Hot Pap Cataplasma

Medically reviewed by Drugs.com. Last updated on Mar 29, 2019.

Dosage form: patch
Ingredients: METHYL SALICYLATE 58.3mg in 13.4g
Labeler: Lydia Co., Ltd.
NDC Code: 72988-0007

Further information

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

Drug Facts

Methyl salicylate

Vanillyl nonylamide

Kaolin

Glycerin

Liquid paraffin

Gelatin

Titanium oxide

Carboxymethylcellulose sodium

Zinc oxide

Methoxyethylene maleicanhydride copolymer

Polybutene

Citric acid hydrate

Sodium polyacrylate

Thymol

Butyl paraben

Butylated hydroxy toluene

Polysorbate 60

Isopropyl myristate

Natural rubber latex

Purified water

Nonwoven fabric

Polyester film

Topical Analgesic

Temporarily relieves minor pain associated with - muscular pain - joint pain - backache - bruise - sprain

keep out of reach of the children

Adults and children 12 years of age and over: apply to affected area not more than 3 to 4 times daily.

Children under 12 years of age: do not use, consult a doctor
For easy application: partially peel back protective film and apply exposed patch to the site of pain.
Carefully remove remaining film while pressing patch to skin for secure adhesion.

use only as directed
do not bandage tightly or use with a healing pad
avoid contact with the eyes and mucous membranes
do not apply to wounds or damaged skin

for external use only

HOT PAP CATAPLASMA 
methyl salicylate, vanillyl nonylamide patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72988-0007
Route of AdministrationTRANSDERMALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (SALICYLIC ACID) METHYL SALICYLATE58.3 mg  in 13.4 g
Inactive Ingredients
Ingredient NameStrength
THYMOL 
KAOLIN 
GLYCERIN 
Packaging
#Item CodePackage Description
1NDC:72988-0007-113.4 g in 1 POUCH
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/29/2019
Labeler - Lydia Co., Ltd. (695735569)
Registrant - Lydia Co., Ltd. (695735569)
Establishment
NameAddressID/FEIOperations
Jeil Health Science Inc.689851513manufacture(72988-0007)
Establishment
NameAddressID/FEIOperations
Lydia Co., Ltd.695735569label(72988-0007)

 
Lydia Co., Ltd.