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  4. NDC Product Code: 52904-962 Dramamine

NDC 52904-962 Dramamine

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 52904-962?
  5. Dramamine Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk
  9. Patient Education

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
52904-962
Proprietary Name:
Dramamine
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Select Corporation
Labeler Code:
52904
Product Label ID:
ec76597c-eb6a-4025-9d64-fb79c2daca51
Start Marketing Date: [9]
01-15-2012
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
ORANGE (C48331)
Shape:
ROUND (C48348)
Size(s):
8 MM
Score:
2
Flavor(s):
ORANGE (C73406)

Code Structure Chart

Product Details

What is NDC 52904-962?

The NDC code 52904-962 is assigned by the FDA to the product Dramamine which is product labeled by Select Corporation. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 52904-962-04 1 pouch in 1 blister pack / 2 tablet in 1 pouch, 52904-962-25 25 pouch in 1 carton / 2 tablet in 1 pouch. 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?

To prevent motion sickness, the first dose should be taken 1/2 to 1 hour before starting activityto prevent or treat motion sickness, see below:adults and children 12 years and overtake 1 to 2 chewable tablets every 4-6 hoursdo not take more than 8 chewable tablets in 24 hours, or as directed by a doctorchildren 6 to under 12 yearsgive 1/2 to 1 chewable tablet every 6-8 hoursdo not give more than 3 chewable tablets in 24 hours, or as directed by a doctorchildren 2 to under 6 yearsgive 1/2 chewable tablet every 6-8 hoursdo not give more than 1½ chewable tablets in 24 hours, or as directed by a doctor

Which are Dramamine UNII Codes?

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

Which are Dramamine 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?

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

Dimenhydrinate


Dimenhydrinate is used to prevent and treat nausea, vomiting, and dizziness caused by motion sickness. Dimenhydrinate is in a class of medications called antihistamines. It works by preventing problems with body balance.
[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".