83602-158 NDC - LIDOCAINE PAIN RELIEF GEL-PATCH (LIDOCAINE)

Drug Information

  • Product NDC: 83602-158
  • Proprietary Name: LIDOCAINE PAIN RELIEF Gel-Patch
  • Non Proprietary Name: Lidocaine
  • Active Ingredient(s): .04 g/g LIDOCAINE.04 g/g LIDOCAINE.04 g/g LIDOCAINE
  • Administration Route(s): TOPICAL
  • Dosage Form(s): PATCH
  • Pharmacy Class(es): Amide Local Anesthetic [EPC]; Amides [CS]; Antiarrhythmic [EPC]; Local Anesthesia [PE]

Labeler Information

Field Name Field Value
Labeler Name: Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
Product Type: HUMAN OTC DRUG
FDA Application Number: M017
Marketing Category: OTC MONOGRAPH DRUG
Start Marketing Date:8/8/2023

Package Information

No. Package Code Package Description Billing Unit
183602-158-0112 g in 1 BAG (83602-158-01)
283602-158-1212 BAG in 1 BOX (83602-158-12) / 12 g in 1 BAG
383602-158-1313 BAG in 1 BOX (83602-158-13) / 12 g in 1 BAG
483602-158-1414 BAG in 1 BOX (83602-158-14) / 12 g in 1 BAG
583602-158-1515 BAG in 1 BOX (83602-158-15) / 12 g in 1 BAG
683602-158-1616 BAG in 1 BOX (83602-158-16) / 12 g in 1 BAG
783602-158-1717 BAG in 1 BOX (83602-158-17) / 12 g in 1 BAG
883602-158-1818 BAG in 1 BOX (83602-158-18) / 12 g in 1 BAG
983602-158-1919 BAG in 1 BOX (83602-158-19) / 12 g in 1 BAG
1083602-158-2020 BAG in 1 BOX (83602-158-20) / 12 g in 1 BAG
1183602-158-2121 BAG in 1 BOX (83602-158-21) / 12 g in 1 BAG
1283602-158-2222 BAG in 1 BOX (83602-158-22) / 12 g in 1 BAG
1383602-158-2323 BAG in 1 BOX (83602-158-23) / 12 g in 1 BAG
1483602-158-2424 BAG in 1 BOX (83602-158-24) / 12 g in 1 BAG
1583602-158-2525 BAG in 1 BOX (83602-158-25) / 12 g in 1 BAG
1683602-158-2626 BAG in 1 BOX (83602-158-26) / 12 g in 1 BAG
1783602-158-2727 BAG in 1 BOX (83602-158-27) / 12 g in 1 BAG
1883602-158-2828 BAG in 1 BOX (83602-158-28) / 12 g in 1 BAG
1983602-158-2929 BAG in 1 BOX (83602-158-29) / 12 g in 1 BAG
2083602-158-3030 BAG in 1 BOX (83602-158-30) / 12 g in 1 BAG
2183602-158-3131 BAG in 1 BOX (83602-158-31) / 12 g in 1 BAG
2283602-158-3232 BAG in 1 BOX (83602-158-32) / 12 g in 1 BAG
2383602-158-3333 BAG in 1 BOX (83602-158-33) / 12 g in 1 BAG
2483602-158-3434 BAG in 1 BOX (83602-158-34) / 12 g in 1 BAG
2583602-158-3535 BAG in 1 BOX (83602-158-35) / 12 g in 1 BAG
2683602-158-3737 BAG in 1 BOX (83602-158-37) / 12 g in 1 BAG
2783602-158-3838 BAG in 1 BOX (83602-158-38) / 12 g in 1 BAG
2883602-158-3939 BAG in 1 BOX (83602-158-39) / 12 g in 1 BAG
2983602-158-4040 BAG in 1 BOX (83602-158-40) / 12 g in 1 BAG
3083602-158-4141 BAG in 1 BOX (83602-158-41) / 12 g in 1 BAG
3183602-158-4242 BAG in 1 BOX (83602-158-42) / 12 g in 1 BAG
3283602-158-4343 BAG in 1 BOX (83602-158-43) / 12 g in 1 BAG
3383602-158-4444 BAG in 1 BOX (83602-158-44) / 12 g in 1 BAG
3483602-158-4545 BAG in 1 BOX (83602-158-45) / 12 g in 1 BAG
3583602-158-4646 BAG in 1 BOX (83602-158-46) / 12 g in 1 BAG

NDC Record

Field Name Field Value Definition
PRODUCT NDC83602-158The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELIDOCAINE PAIN RELIEF Gel-PatchThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMELidocaineThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPATCHThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/3/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERM017This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMELIDOCAINEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.04 
ACTIVE INGRED UNITg/g 
PHARM CLASSESAmide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] 
PRODUCT NDC83602-158The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELIDOCAINE PAIN RELIEF Gel-PatchThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMELidocaineThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPATCHThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/8/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERM017This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMELIDOCAINEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.04 
ACTIVE INGRED UNITg/g 
PHARM CLASSESAmide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] 
PRODUCT NDC83602-158The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELIDOCAINE PAIN RELIEF Gel-PatchThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMELidocaineThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEPATCHThe translation of the dosage form Code submitted by the firm.
ROUTE NAMETOPICALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE8/8/2023This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
APPLICATION NUMBERM017This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.
LABELER NAMEGuangzhou Liuquanmiao Import & Export Trade Co., Ltd.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMELIDOCAINEAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH.04 
ACTIVE INGRED UNITg/g 
PHARM CLASSESAmide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE] 

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This page was last updated on: 11/21/2025

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