NDC Package 0031-2102-01 Robitussin Childrens Honey Day Night Dm Value Pack

Dextromethorphan Hbr,Guaifenesin,Doxylamine Succinate Kit - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
0031-2102-01
Package Description:
1 KIT in 1 CARTON * 1 BOTTLE in 1 CARTON (0031-8760-12) / 118 mL in 1 BOTTLE * 1 BOTTLE in 1 CARTON (0031-8762-12) / 118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Robitussin Childrens Honey Day Night Dm Value Pack
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifenesin, Doxylamine Succinate
Usage Information:
▪do not take more than 6 doses in any 24-hour period▪measure only with dosing cup provided▪keep dosing cup with product▪mL = milliliteragedosechildren under 4 yearsdo not usechildren 4 to under 6 years5 mL every 4 hourschildren 6 to under 12 years10 mL every 4 hoursadults and children 12 years and over20 mL every 4 hours
11-Digit NDC Billing Format:
00031210201
NDC to RxNorm Crosswalk:
  • RxCUI: 1115329 - dextromethorphan HBr 30 MG / doxylamine succinate 12.5 MG in 20 mL Oral Solution
  • RxCUI: 1115329 - dextromethorphan hydrobromide 1.5 MG/ML / doxylamine succinate 0.625 MG/ML Oral Solution
  • RxCUI: 1115329 - dextromethorphan hydrobromide 30 MG / doxylamine succinate 12.5 MG per 20 ML Oral Solution
  • RxCUI: 1115329 - dextromethorphan hydrobromide 7.5 MG / doxylamine succinate 3.125 MG per 5 ML Oral Solution
  • RxCUI: 1790650 - dextromethorphan HBr 10 MG / guaiFENesin 100 MG in 10 mL Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
Haleon Us Holdings Llc
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
05-27-2019
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

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 NDC 0031-2102-01?

The NDC Packaged Code 0031-2102-01 is assigned to a package of 1 kit in 1 carton * 1 bottle in 1 carton (0031-8760-12) / 118 ml in 1 bottle * 1 bottle in 1 carton (0031-8762-12) / 118 ml in 1 bottle of Robitussin Childrens Honey Day Night Dm Value Pack, a human over the counter drug labeled by Haleon Us Holdings Llc. The product's dosage form is kit and is administered via form.

Is NDC 0031-2102 included in the NDC Directory?

Yes, Robitussin Childrens Honey Day Night Dm Value Pack with product code 0031-2102 is active and included in the NDC Directory. The product was first marketed by Haleon Us Holdings Llc on May 27, 2019 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0031-2102-01?

The 11-digit format is 00031210201. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 4-4-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
4-4-20031-2102-015-4-200031-2102-01