69538-100 NDC - WIPE N GO ()

Drug Information

Product NDC: 69538-100

Proprietary Name: Wipe n Go

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: CANADIA USA CORPORATION
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/21/2015

Package Information

No. Package Code Package Description Billing Unit
169538-100-0136 PACKAGE in 1 BOX (69538-100-01) / 8 PACKET in 1 PACKAGE / 3 g in 1 PACKET
269538-100-024 CARTON in 1 BOX (69538-100-02) / 10 PACKAGE in 1 CARTON / 8 PACKET in 1 PACKAGE / 3 g in 1 PACKET
369538-100-038 CARTON in 1 BOX (69538-100-03) / 10 PACKAGE in 1 CARTON / 8 PACKET in 1 PACKAGE / 3 g in 1 PACKET
469538-100-0412 CARTON in 1 BOX (69538-100-04) / 10 PACKAGE in 1 CARTON / 8 PACKET in 1 PACKAGE / 3 g in 1 PACKET

NDC Record

Field Name Field Value Definition
PRODUCT NDC69538-100The 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 NAMEWipe n GoThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/21/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECANADIA USA CORPORATIONName 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