NDC 68071-4595 Motion-time Chewable

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:
68071-4595
Proprietary Name:
Motion-time Chewable
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Nucare Pharmaceuticals,inc.
Labeler Code:
68071
Start Marketing Date: [9]
08-09-2010
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
PINK (C48328)
Shape:
ROUND (C48348)
Size(s):
9 MM
Imprint(s):
TCL333
Score:
2
Flavor(s):
RASPBERRY (C73413)

Product Packages

NDC Code 68071-4595-2

Package Description: 20 TABLET, CHEWABLE in 1 BOTTLE

NDC Code 68071-4595-3

Package Description: 30 TABLET, CHEWABLE in 1 BOTTLE

NDC Code 68071-4595-4

Package Description: 40 TABLET, CHEWABLE in 1 BOTTLE

NDC Code 68071-4595-6

Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE

Product Details

What is NDC 68071-4595?

The NDC code 68071-4595 is assigned by the FDA to the product Motion-time Chewable which is product labeled by Nucare Pharmaceuticals,inc.. The product's dosage form is . The product is distributed in 4 packages with assigned NDC codes 68071-4595-2 20 tablet, chewable in 1 bottle , 68071-4595-3 30 tablet, chewable in 1 bottle , 68071-4595-4 40 tablet, chewable in 1 bottle , 68071-4595-6 60 tablet, chewable in 1 bottle . 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 Motion-time Chewable?

Uses prevents and treats nausea, vomiting, or dizziness associated with motion sickness.

Which are Motion-time Chewable UNII Codes?

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

Which are Motion-time Chewable 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 Motion-time Chewable?

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:

* Please review the disclaimer below.

Patient Education

Meclizine


Meclizine is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. It is most effective if taken before symptoms appear.
[Learn More]


* Please review the disclaimer below.

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".