82442-745 NDC - UP UP (PAIN RELIEF ADVANCED HYDROGEL PATCHES)

Drug Information

Product NDC: 82442-745
Proprietary Name: Up up
Non Proprietary Name: Pain Relief Advanced Hydrogel Patches
Active Ingredient(s): 110 mg/1000mg CAMPHOR (SYNTHETIC); 22 mg/1000mg CAPSICUM; 33 mg/1000mg LEVOMENTHOL
Administration Route(s): TOPICAL
Dosage Form(s): PATCH
Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Dietary Proteins [CS]; Increased Histamine Release [PE]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Plant Proteins [CS]; Vegetable Proteins [CS]

Labeler Information

Field Name	Field Value
Labeler Name:	Target Corporation
Product Type:	HUMAN OTC DRUG
FDA Application Number:	M017
Marketing Category:	OTC MONOGRAPH DRUG
Start Marketing Date:	11/21/2025

Package Information

No.	Package Code	Package Description	Billing Unit
1	82442-745-05	5000 mg in 1 POUCH (82442-745-05)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	82442-745	The 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 NAME	HUMAN OTC DRUG	Indicates 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 NAME	Up up	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Pain Relief Advanced Hydrogel Patches	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	PATCH	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	TOPICAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	11/21/2025	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	OTC MONOGRAPH DRUG	Product 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 NUMBER	M017	This 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 NAME	Target Corporation	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	CAMPHOR (SYNTHETIC); CAPSICUM; LEVOMENTHOL	An 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	110; 22; 33
ACTIVE INGRED UNIT	mg/1000mg; mg/1000mg; mg/1000mg
PHARM CLASSES	Allergens [CS], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Vegetable Proteins [CS]

82442-745 NDC - UP UP (PAIN RELIEF ADVANCED HYDROGEL PATCHES)

Drug Information

Labeler Information

Package Information

NDC Record

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