51879-122 NDC - LICEFREEE (SODIUM CHLORIDE)

Drug Information

Product NDC: 51879-122

Proprietary Name: Licefreee

Non Proprietary Name: Sodium chloride

Active Ingredient(s):


Administration Route(s): TOPICAL

Dosage Form(s): KIT

Labeler Information

Labeler Name: Tec Laboratories, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/13/2016

Package Information

No. Package Code Package Description Billing Unit
151879-122-881 KIT in 1 KIT (51879-122-88) * 227 g in 1 BOTTLE, PLASTIC (51879-121-80) * 236.6 mL in 1 BOTTLE, PLASTIC (51879-191-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC51879-122The 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 NAMELicefreeeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMESodium chlorideThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEKITThe 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 DATE7/13/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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 NAMETec Laboratories, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023