73715-005 NDC - DICLOFENAC SODIUM TOPICAL GEL, 1% (DICLOFENAC SODIUM TOPICAL GEL, 1% (NSAID))

Drug Information

Product NDC: 73715-005
Proprietary Name: Diclofenac Sodium Topical Gel, 1%
Non Proprietary Name: Diclofenac Sodium Topical Gel, 1% (NSAID)
Active Ingredient(s): 1 g/100g DICLOFENAC SODIUM
Administration Route(s): TOPICAL
Dosage Form(s): GEL
Pharmacy Class(es): Anti-Inflammatory Agents; Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Decreased Prostaglandin Production [PE]; Nonsteroidal Anti-inflammatory Drug [EPC]

Labeler Information

Field Name	Field Value
Labeler Name:	Mohnark Pharmaceuticals Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED DRUG OTHER
Start Marketing Date:	8/31/2021

Package Information

No.	Package Code	Package Description	Billing Unit
1	73715-005-01	50 g in 1 CARTON (73715-005-01)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	73715-005	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	Diclofenac Sodium Topical Gel, 1%	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	Diclofenac Sodium Topical Gel, 1% (NSAID)	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	GEL	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	8/31/2021	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED DRUG OTHER	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.
LABELER NAME	Mohnark Pharmaceuticals Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	DICLOFENAC SODIUM	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	1
ACTIVE INGRED UNIT	g/100g
PHARM CLASSES	Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC]

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This page was last updated on: 5/26/2025

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