HOT PAP CATAPLASMA- methyl salicylate, vanillyl nonylamide patch 
Lydia Co., Ltd.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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

label

HOT PAP CATAPLASMA 
methyl salicylate, vanillyl nonylamide patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72988-0007
Route of AdministrationTRANSDERMAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE58.3 mg  in 13.4 g
NONIVAMIDE (UNII: S846B891OR) (NONIVAMIDE - UNII:S846B891OR) NONIVAMIDE5 mg  in 13.4 g
Inactive Ingredients
Ingredient NameStrength
THYMOL (UNII: 3J50XA376E)  
KAOLIN (UNII: 24H4NWX5CO)  
GLYCERIN (UNII: PDC6A3C0OX)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:72988-0007-25 in 1 PACKAGE03/29/2019
1NDC:72988-0007-113.4 g in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other03/29/2019
Labeler - Lydia Co., Ltd. (695735569)
Registrant - Lydia Co., Ltd. (695735569)
Establishment
NameAddressID/FEIBusiness Operations
Lydia Co., Ltd.695735569label(72988-0007) , manufacture(72988-0007)

Revised: 7/2023
Document Id: ffc8f035-939b-481a-e053-6294a90a5b61
Set id: 85360782-69cc-ba9e-e053-2a91aa0a5431
Version: 3
Effective Time: 20230705
 
Lydia Co., Ltd.