Panadol Tablet
NDC Package 0135-7033-20
Package Information
Panadol (acetaminophen, dextromethorphan hbr) tablets is do not use more than directedadults and children 12 years of age and over: take 2 caplets every 6 hours, while symptoms persistdo not take more than 6 caplets in 24 hours unless directed by a doctorchildren under 12 years of age: do not useAgeDoseadults and children 12 years of age and over2 caplets every 6 hourschildren under 12 years of agedo not use. This formulation utilizes a tablet delivery system. Marketed by Haleon Us Holdings Llc, this product is identified by NDC 0135-7033 and is authorized under FDA application M012.
Identification & Billing
- RxCUI: 247324 - acetaminophen 500 MG /dextromethorphan HBr 15 MG Oral Tablet
- RxCUI: 247324 - acetaminophen 500 MG / dextromethorphan hydrobromide 15 MG Oral Tablet
- RxCUI: 247324 - APAP 500 MG / Dextromethorphan Hydrobromide 15 MG Oral Tablet
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0135 - Haleon Us Holdings Llc
- 0135-7033 - Panadol
- 0135-7033-20 - 2 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
- 0135-7033 - Panadol
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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Other Available Packages
The following commercial packages are registered under the same Product NDC (0135-7033). 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 0135-7033-20 identifies a specific commercial package of 2 blister pack in 1 carton / 10 tablet in 1 blister pack of Panadol Cold And Flu Day, a human over the counter drug labeled by Haleon Us Holdings Llc. This tablet is formulated for oral use and contains acetaminophen; dextromethorphan hydrobromide 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 Haleon Us Holdings Llc on April 30, 2026. The current certification is valid through December 31, 2027.
How is this Haleon Us Holdings Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00135703320. 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.