Label: HOT PAP CATAPLASMA- methyl salicylate, vanillyl nonylamide patch
- NDC Code(s): 72988-0007-1, 72988-0007-2
- Packager: Lydia Co., Ltd.
- Category: HUMAN OTC DRUG LABEL
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.
Drug Label Information
Updated July 5, 2023
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- Official Label (Printer Friendly)
- ACTIVE INGREDIENT
-
INACTIVE INGREDIENT
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
- PURPOSE
- KEEP OUT OF REACH OF CHILDREN
-
INDICATIONS & USAGE
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. - WARNINGS
- DOSAGE & ADMINISTRATION
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
HOT PAP CATAPLASMA
methyl salicylate, vanillyl nonylamide patchProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:72988-0007 Route of Administration TRANSDERMAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 58.3 mg in 13.4 g NONIVAMIDE (UNII: S846B891OR) (NONIVAMIDE - UNII:S846B891OR) NONIVAMIDE 5 mg in 13.4 g Inactive Ingredients Ingredient Name Strength THYMOL (UNII: 3J50XA376E) KAOLIN (UNII: 24H4NWX5CO) GLYCERIN (UNII: PDC6A3C0OX) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:72988-0007-2 5 in 1 PACKAGE 03/29/2019 1 NDC:72988-0007-1 13.4 g in 1 PATCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 03/29/2019 Labeler - Lydia Co., Ltd. (695735569) Registrant - Lydia Co., Ltd. (695735569) Establishment Name Address ID/FEI Business Operations Lydia Co., Ltd. 695735569 label(72988-0007) , manufacture(72988-0007)