59262-502 NDC - BABY GUM RELIEF ()

Drug Information

Product NDC: 59262-502

Proprietary Name: BABY GUM RELIEF

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Similasan Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/15/2018

Package Information

No. Package Code Package Description Billing Unit
159262-502-261 BOTTLE in 1 BOX (59262-502-26) / 135 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC59262-502The 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 NAMEBABY GUM 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 DATE6/15/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESimilasan 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