0363-0449 NDC - JUNIOR PAIN RELIEVIER ()

Drug Information

  • Product NDC: 0363-0449
  • Proprietary Name: Junior Pain Relievier
  • Non Proprietary Name:
  • Active Ingredient(s): 1800 mg/1 GLYCERIN
  • Administration Route(s):
  • Dosage Form(s):
  • Pharmacy Class(es): Allergens [CS]; Cell-mediated Immunity [PE]; Glycerol [CS]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Non-Standardized Chemical Allergen [EPC]

Labeler Information

Field Name Field Value
Labeler Name: WALGREEN CO.
Product Type:
FDA Application Number: part343
Marketing Category: OTC MONOGRAPH NOT FINAL
Start Marketing Date:1/28/2005
End Marketing Date:8/19/2013

Package Information

No. Package Code Package Description Billing Unit
10363-0449-0020 BLISTER PACK in 1 CARTON (0363-0449-00) / 5 SUPPOSITORY in 1 BLISTER PACK
20363-0449-081 BLISTER PACK in 1 CARTON (0363-0449-08) / 24 TABLET, CHEWABLE in 1 BLISTER PACKEA
30363-0449-255 BLISTER PACK in 1 CARTON (0363-0449-25) / 5 SUPPOSITORY in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC0363-0449The 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.
PROPRIETARY NAMEJunior Pain RelievierThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/28/2005This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH NOT FINALProduct 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 NUMBERpart343This 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 NAMEWALGREEN CO.Name of Company corresponding to the labeler code segment of the Product NDC.
PRODUCT NDC0363-0449The 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.
PROPRIETARY NAMEWALGREEN GLYCERIN ADULTThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/25/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEOTC MONOGRAPH DRUGProduct 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 NUMBERM007This 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 NAMEWalgreensName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 11/21/2025

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