0219-6103 NDC - HUMPHREYS BABY TEETHING RELIEF ORIGINAL ()

Drug Information

Product NDC: 0219-6103

Proprietary Name: Humphreys Baby Teething Relief Original

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Humphreys Pharmacal, Incorporated
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	3/1/2011

No.	Package Code	Package Description	Billing Unit
1	0219-6103-00	1 BOTTLE, PLASTIC in 1 CARTON (0219-6103-00) / 135 PELLET in 1 BOTTLE, PLASTIC

Field Name	Field Value	Definition
PRODUCT NDC	0219-6103	The 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 NAME	Humphreys Baby Teething Relief Original	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	3/1/2011	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Humphreys Pharmacal, Incorporated	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