Onessip Day Time Kids Cold And Cough Plus Fever Liquid
NDC Package 87078-331-16

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

Package Information

Onessip Day Time Kids Cold And Cough Plus Fever (acetaminophen 325 mg and dextromethorphan hbr 10 mg oral liquid day time kids) liquids is take only as directeddo not exceed 4 doses per 24 hrsdo not give more than directed (see liver warning)follow the instruction given on this carton for your eash usemL=mililiterAge (years)Dose (Sachet)Adults & Children 12 yrs & Over2 sachets (20 mL*) every 4 hrsChildren 6 to under 12 yrs1 sachet (10 mL*) every 4 hrsChildren 4 to under 6 yrsask a doctorChildren under 4 yrsdo not use. This formulation utilizes a liquid delivery system. Marketed by Medwise Lifesciences Inc., this product is identified by NDC 87078-331 and is authorized under FDA application M012.

Identification & Billing

NDC Package Code
87078-331-16
Package Description
16 POUCH in 1 CARTON / 10 mL in 1 POUCH (87078-331-01)
Product Code
11-Digit Billing Format
87078033116
RxNorm Crosswalk
  • RxCUI: 1919076 - acetaminophen 325 MG / dextromethorphan HBr 10 MG in 10 mL Oral Solution
  • RxCUI: 1919076 - acetaminophen 32.5 MG/ML / dextromethorphan hydrobromide 1 MG/ML Oral Solution
  • RxCUI: 1919076 - acetaminophen 325 MG / dextromethorphan HBr 10 MG per 10 mL Oral Solution
  • RxCUI: 1919076 - acetaminophen 650 MG / dextromethorphan HBr 20 MG per 20 mL Oral Solution
  • RxCUI: 1919076 - APAP 32.5 MG/ML / Dextromethorphan Hydrobromide 1 MG/ML Oral Solution

Clinical Specifications

Proprietary Name
Onessip Day Time Kids Cold And Cough Plus Fever
Non-Proprietary Name
Acetaminophen 325 Mg And Dextromethorphan Hbr 10 Mg Oral Liquid Day Time Kids
Substance Name
Acetaminophen; Dextromethorphan Hydrobromide
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Usage Information
Take only as directeddo not exceed 4 doses per 24 hrsdo not give more than directed (see liver warning)follow the instruction given on this carton for your eash usemL=mililiterAge (years)Dose (Sachet)Adults & Children 12 yrs & Over2 sachets (20 mL*) every 4 hrsChildren 6 to under 12 yrs1 sachet (10 mL*) every 4 hrsChildren 4 to under 6 yrsask a doctorChildren under 4 yrsdo not use

Regulatory & Marketing

Labeler Name
Medwise Lifesciences Inc.
Product Type
Human Otc Drug
FDA Application #
M012
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-15-2026
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 87078-331-16 identifies a specific commercial package of 16 pouch in 1 carton / 10 ml in 1 pouch (87078-331-01) of Onessip Day Time Kids Cold And Cough Plus Fever, a human over the counter drug labeled by Medwise Lifesciences Inc.. This liquid 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 Medwise Lifesciences Inc. on May 15, 2026. The current certification is valid through December 31, 2027.

How is this Medwise Lifesciences Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87078033116. 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)
87078-331-16
11-Digit CMS (5-4-2)
87078-0331-16

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