0363-1095 NDC - WALGREENS MEDICATED FRUIT GUMMIES (ZINCUM ACETICUM ZICUM GLUCONICUM)

Drug Information

Product NDC: 0363-1095

Proprietary Name: Walgreens Medicated Fruit Gummies

Non Proprietary Name: Zincum Aceticum Zicum Gluconicum

Active Ingredient(s):
  • 2 [hp_X]/1 ZINC ACETATE;
  • 2 [hp_X]/1 ZINC GLUCONATE


Administration Route(s): ORAL

Dosage Form(s): TABLET, CHEWABLE

Labeler Information

Labeler Name: Walgreen
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:3/29/2019

Package Information

No. Package Code Package Description Billing Unit
10363-1095-2525 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0363-1095-25)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0363-1095The 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 NAMEWalgreens Medicated Fruit GummiesThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEZincum Aceticum Zicum GluconicumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMETABLET, CHEWABLEThe 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 DATE3/29/2019This 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 NAMEWalgreenName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEZINC ACETATE; ZINC GLUCONATEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH2; 2 
ACTIVE INGRED UNIT[hp_X]/1; [hp_X]/1 

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This page was last updated on: 10/4/2019