Equate Daytime Severe Vaporice Cold And Flu Nighttime Severe Vapor Ice Cold And Flu Kit
NDC Package 49035-796-02

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Equate Daytime Severe Vaporice Cold And Flu Nighttime Severe Vapor Ice Cold And Flu (acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, doxylamine succinate) kits is •take only as directed - see overdose warning•do not exceed 8 caplets per 24 hrsadults & children 12 yrs & over2 caplets with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use •take only as directed - see overdose warning•do not exceed 8 caplets per 24 hrsadults & children 12 yrs & over2 caplets with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use. This formulation utilizes a kit delivery system. Marketed by Wal-mart Stores Inc, this product is identified by NDC 49035-796 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
49035-796-02
Package Description
1 KIT in 1 CARTON * 8 BLISTER PACK in 1 KIT / 2 TABLET, FILM COATED in 1 BLISTER PACK * 4 BLISTER PACK in 1 KIT / 2 TABLET, FILM COATED in 1 BLISTER PACK
Product Code
11-Digit Billing Format
49035079602
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
RxNorm Crosswalk
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / guaiFENesin 200 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1110988 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1110988 - APAP 325 MG / dextromethorphan hydrobromide 10 MG / guaifenesin 200 MG / phenylephrine hydrochloride 5 MG Oral Tablet
  • RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan HBr 10 MG / doxylamine succinate 6.25 MG / phenylephrine HCl 5 MG Oral Tablet
  • RxCUI: 1546881 - acetaminophen 325 MG / dextromethorphan hydrobromide 10 MG / doxylamine succinate 6.25 MG / phenylephrine hydrochloride 5 MG Oral Tablet

Clinical Specifications

Proprietary Name
Equate Daytime Severe Vaporice Cold And Flu Nighttime Severe Vapor Ice Cold And Flu
Non-Proprietary Name
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, Doxylamine Succinate
Dosage Form
Kit - A packaged collection of related material.
Usage Information
•take only as directed - see overdose warning•do not exceed 8 caplets per 24 hrsadults & children 12 yrs & over2 caplets with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use •take only as directed - see overdose warning•do not exceed 8 caplets per 24 hrsadults & children 12 yrs & over2 caplets with water every 4 hrschildren 4 to under 12 yrsask a doctorchildren under 4 yrsdo not use

Regulatory & Marketing

Labeler Name
Wal-mart Stores Inc
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-14-2020
Listing Expiration
12-31-2027
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 49035-796-02 identifies a specific commercial package of 1 kit in 1 carton * 8 blister pack in 1 kit / 2 tablet, film coated in 1 blister pack * 4 blister pack in 1 kit / 2 tablet, film coated in 1 blister pack of Equate Daytime Severe Vaporice Cold And Flu Nighttime Severe Vapor Ice Cold And Flu, a human over the counter drug labeled by Wal-mart Stores Inc. This kit is formulated for use and contains 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 July 14, 2020. 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: 49035079602. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. 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 (5-3-2)
49035-796-02
11-Digit CMS (5-4-2)
49035-0796-02

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