Dimenhydrinate
NDC Package 0924-1007-02
Package Information
Dimenhydrinate is to prevemt motion sickness the first dose should be taken ½ to 1 hour before starting activity.To prevent or treat motion sickness:Adults and Children (12 years and older)take 1-2 tablets every 4-6 hours, not more than 8 tablets in 24 hours, or as directed by doctor.Children 6 to under 12 yearsgive 1 tablet every 6-8 hours, not more than 3 tablets in 24 hours or as directed by doctor.Children 2 to under 6 yearsgive ¼ to ½ tablet every 6-8 hours, not more than 1½ tablets in 24 hours or as directed by a doctor. Marketed by Acme United Corporation, this product is identified by NDC 0924-1007 and is authorized under FDA application part336.
Identification & Billing
- RxCUI: 198603 - dimenhyDRINATE 50 MG Oral Tablet
- RxCUI: 198603 - dimenhydrinate 50 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0924 - Acme United Corporation
- 0924-1007 - Dimenhydrinate
- 0924-1007-02 - 6 PACKET in 1 BAG / 2 TABLET in 1 PACKET
- 0924-1007 - Dimenhydrinate
The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.
* Please review the full disclaimer at the bottom of this page.
Other Available Packages
The following commercial packages are registered under the same Product NDC (0924-1007). Click a package code to view its specific billing and regulatory data.
* Please review the full disclaimer at the bottom of this page.
Frequently Asked Questions
What is the distribution configuration for this product package?
The code 0924-1007-02 identifies a specific commercial package of 6 packet in 1 bag / 2 tablet in 1 packet of Dimenhydrinate, labeled by Acme United Corporation. This is formulated for use and contains as the active substance.
Is this product currently listed with the FDA?
This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Acme United Corporation on April 18, 2019. The current certification is valid through December 31, 2022.
How is this Acme United Corporation product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00924100702. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.
11-Digit Code Conversion
Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.