73824-001 NDC - DEWS PLUS ()

Drug Information

Product NDC: 73824-001

Proprietary Name: Dews Plus

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: DP IMPORT & EXPORT, INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/13/2020

Package Information

No. Package Code Package Description Billing Unit
173824-001-0110 mL in 1 POUCH (73824-001-01)
273824-001-0215 mL in 1 POUCH (73824-001-02)
373824-001-0330 mL in 1 POUCH (73824-001-03)
473824-001-0450 mL in 1 POUCH (73824-001-04)
573824-001-0560 mL in 1 POUCH (73824-001-05)
673824-001-0690 mL in 1 POUCH (73824-001-06)
773824-001-07100 mL in 1 POUCH (73824-001-07)
873824-001-08120 mL in 1 BOTTLE (73824-001-08)
973824-001-09125 mL in 1 BOTTLE (73824-001-09)
1073824-001-10150 mL in 1 BOTTLE (73824-001-10)
1173824-001-11180 mL in 1 BOTTLE (73824-001-11)
1273824-001-12237 mL in 1 BOTTLE (73824-001-12)
1373824-001-13240 mL in 1 BOTTLE (73824-001-13)
1473824-001-14360 mL in 1 BOTTLE (73824-001-14)
1573824-001-15480 mL in 1 BOTTLE (73824-001-15)
1673824-001-16500 mL in 1 BOTTLE (73824-001-16)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73824-001The 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 NAMEDews PlusThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/13/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDP IMPORT & EXPORT, 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