59726-041 NDC - ALL DAY ALLERGY RELIEF ()

Drug Information

Product NDC: 59726-041

Proprietary Name: All Day Allergy Relief

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: P & L Development, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/31/2018

Package Information

No. Package Code Package Description Billing Unit
159726-041-101 BOTTLE in 1 BOX (59726-041-10) / 10 CAPSULE in 1 BOTTLE
259726-041-121 BOTTLE in 1 BOX (59726-041-12) / 12 CAPSULE in 1 BOTTLE
359726-041-251 BOTTLE in 1 BOX (59726-041-25) / 25 CAPSULE in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC59726-041The 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 NAMEAll Day Allergy ReliefThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/31/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEP & L Development, LLCName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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