NDC 63029-904 Dramamine For Kids

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:
63029-904
Proprietary Name:
Dramamine For Kids
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Medtech Products Inc.
Labeler Code:
63029
Start Marketing Date: [9]
02-15-2012
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
10 MM
Imprint(s):
DRA
Score:
2
Flavor(s):
GRAPE (C73391)

Product Packages

NDC Code 63029-904-01

Package Description: 1 CASE in 1 BLISTER PACK / 8 TABLET, CHEWABLE in 1 CASE

Product Details

What is NDC 63029-904?

The NDC code 63029-904 is assigned by the FDA to the product Dramamine For Kids which is product labeled by Medtech Products Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 63029-904-01 1 case in 1 blister pack / 8 tablet, chewable in 1 case. 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 Dramamine For Kids?

To prevent motion sickness, the first dose should be taken ½ to 1 hour before starting activityto prevent or treat motion sickness, see below:Children 2to under 6yearsgive ½ to 1 chewable tablet every 6-8 hoursdo not give more than 3 chewable tabletsin 24 hours, or as directed by a doctorChildren 6to under 12yearsgive 1 to 2 chewable tablets every 6-8 hoursdo not give more than 6 chewable tablets in24 hours, or as directed by a doctor

Which are Dramamine For Kids UNII Codes?

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

Which are Dramamine For Kids 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:

What is the NDC to RxNorm Crosswalk for Dramamine For Kids?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".