Advil Pm Capsule, Liquid Filled
NDC Package 0573-0167-55

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Advil Pm (diphenhydramine hcl, ibuprofen) capsules is do not take more than directedadults and children 12 years and over: take 2 capsules at bedtimedo not take more than 2 capsules in 24 hours. This formulation utilizes a capsule, liquid filled delivery system. Marketed by Haleon Us Holdings Llc, this product is identified by NDC 0573-0167 and is authorized under FDA application NDA021393.

Identification & Billing

NDC Package Code
0573-0167-55
Package Description
1 BOTTLE in 1 CARTON / 80 CAPSULE, LIQUID FILLED in 1 BOTTLE
Product Code
0573-0167
11-Digit Billing Format
00573016755
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
1 EA
RxNorm Crosswalk
  • RxCUI: 901814 - ibuprofen 200 MG / diphenhydrAMINE HCl 25 MG Oral Capsule
  • RxCUI: 901814 - diphenhydramine hydrochloride 25 MG / ibuprofen 200 MG Oral Capsule

Clinical Specifications

Proprietary Name
Advil Pm
Non-Proprietary Name
Diphenhydramine Hcl, Ibuprofen
Substance Name
Diphenhydramine Hydrochloride; Ibuprofen
Dosage Form
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Do not take more than directedadults and children 12 years and over: take 2 capsules at bedtimedo not take more than 2 capsules in 24 hours

Regulatory & Marketing

Labeler Name
Haleon Us Holdings Llc
Product Type
Human Otc Drug
FDA Application #
NDA021393
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
12-20-2005
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 (0573-0167). Click a package code to view its specific billing and regulatory data.

0573-0167-10
16 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
0573-0167-18
24 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
0573-0167-19
24 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
0573-0167-20
32 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
0573-0167-21
40 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
0573-0167-25
1 BOTTLE in 1 CARTON / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE
0573-0167-26
1 BOTTLE in 1 CARTON / 30 CAPSULE, LIQUID FILLED in 1 BOTTLE
0573-0167-42
40 BLISTER PACK in 1 CARTON / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
0573-0167-43
1 BOTTLE in 1 CARTON / 40 CAPSULE, LIQUID FILLED in 1 BOTTLE
0573-0167-44
1 BOTTLE in 1 CARTON / 50 CAPSULE, LIQUID FILLED in 1 BOTTLE
0573-0167-56
1 BOTTLE in 1 CARTON / 100 CAPSULE, LIQUID FILLED in 1 BOTTLE

* 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 0573-0167-55 identifies a specific commercial package of 1 bottle in 1 carton / 80 capsule, liquid filled in 1 bottle of Advil Pm, a human over the counter drug labeled by Haleon Us Holdings Llc. This capsule, liquid filled is formulated for oral use and contains diphenhydramine hydrochloride; ibuprofen 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 December 20, 2005. The current certification is valid through December 31, 2026.

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: 00573016755. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 1 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:

10-Digit Format (4-4-2)
0573-0167-55
11-Digit CMS (5-4-2)
00573-0167-55

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.