62011-0302 NDC - HEALTH MART MUCUS RELIEF DM (DEXTROMETHORPHAN HBR, GUAIFENESIN)

Drug Information

Product NDC: 62011-0302

Proprietary Name: Health Mart mucus relief DM

Non Proprietary Name: Dextromethorphan HBr, Guaifenesin

Active Ingredient(s):
  • 60 mg/1 DEXTROMETHORPHAN HYDROBROMIDE;
  • 1200 mg/1 GUAIFENESIN


Administration Route(s): ORAL

Dosage Form(s): TABLET, EXTENDED RELEASE

Labeler Information

Labeler Name: Strategic Sourcing Services LLC
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA091070
Marketing Category: ANDA
Start Marketing Date:7/11/2016

Package Information

No. Package Code Package Description Billing Unit
162011-0302-11 BOTTLE in 1 CARTON (62011-0302-1) > 14 TABLET, EXTENDED RELEASE in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC62011-0302The 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 NAMEHealth Mart mucus relief DMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEDextromethorphan HBr, GuaifenesinThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, EXTENDED RELEASEThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE7/11/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEANDAProduct 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 NUMBERANDA091070This 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 NAMEStrategic Sourcing Services LLCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEDEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESINThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH60; 1200 
ACTIVE INGRED UNITmg/1; mg/1 

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This page was last updated on: 11/18/2019