NDC 0219-3103 Humphreys Baby Teething Relief Very Cherry

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
0219-3103
Proprietary Name:
Humphreys Baby Teething Relief Very Cherry
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Humphreys Pharmacal, Incorporated
Labeler Code:
0219
Start Marketing Date: [9]
01-01-2012
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
CHERRY (C73375 - NATURAL FRUIT FLAVOR)

Product Packages

NDC Code 0219-3103-00

Package Description: 1 BOTTLE, PLASTIC in 1 CARTON / 135 PELLET in 1 BOTTLE, PLASTIC

Product Details

What is NDC 0219-3103?

The NDC code 0219-3103 is assigned by the FDA to the product Humphreys Baby Teething Relief Very Cherry which is product labeled by Humphreys Pharmacal, Incorporated. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0219-3103-00 1 bottle, plastic in 1 carton / 135 pellet in 1 bottle, plastic. This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Humphreys Baby Teething Relief Very Cherry?

Place 1 to 3 pellets in 1/2 teaspoon of water and allow to dissolve.After dissolving, apply to child's gums. If needed, repeat every 2 hoursup to 4 times per day. If preferred, mixture may be administered under the tongue.If child is persistently irritable wakeful and restless, administer 3 pellets before bed- repeat if necessary or as directed by a healthcare professional.

Which are Humphreys Baby Teething Relief Very Cherry UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Humphreys Baby Teething Relief Very Cherry Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".