Motion Sickness Relief Tablet
NDC Package 49035-981-12
Package Information
Motion Sickness Relief (dimenhydrinate) tablets is do not take more than directedto 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 tablets every 4-6 hoursdo not take more than 8 tablets in 24 hours, or as directed by a doctorchildren 6 to under 12 yearsgive 1/2 to 1 tablet every 6-8 hoursdo not give more than 3 tablets in 24 hours, or as directed by a doctorchildren 2 to under 6 yearsgive 1/2 tablet every 6-8 hoursdo not give more than 1 1/2 tablets in 24 hours, or as directed by a doctor. This formulation utilizes a tablet delivery system. Marketed by Wal-mart Stores Inc, this product is identified by NDC 49035-981 and is authorized under FDA application M009.
Identification & Billing
- RxCUI: 198603 - dimenhyDRINATE 50 MG Oral Tablet
- RxCUI: 198603 - dimenhydrinate 50 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 49035 - Wal-mart Stores Inc
- 49035-981 - Motion Sickness Relief
- 49035-981-12 - 100 TABLET in 1 BOTTLE, PLASTIC
- 49035-981 - Motion Sickness Relief
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 49035-981-12 identifies a specific commercial package of 100 tablet in 1 bottle, plastic of Motion Sickness Relief, a human over the counter drug labeled by Wal-mart Stores Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 100 billable units per package. This tablet is formulated for oral use and contains dimenhydrinate as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Wal-mart Stores Inc on December 01, 1992. The current certification is valid through December 31, 2027.
How is this Wal-mart Stores Inc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 49035098112. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 100 total billable units per package. 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 Product segment to maintain the 5-4-2 structure.