NDC Package 49580-0294-4 Mucus Relief Cough Childrens

Dextromethorphan Hbr,Guaifensin Liquid Oral - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
49580-0294-4
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 118 mL in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Mucus Relief Cough Childrens
Non-Proprietary Name:
Dextromethorphan Hbr, Guaifensin
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Do not take more than 6 doses in any 24-hour period measure only with dosing cup provided. Do not use any other dosing device. keep dosing cup with product mL = milliliter shake well before usingage dose  children 6 to 12 years  5-10 mL every 4 hours  children 4 to 5 years 2.5-5 mL every 4 hours children under 4 years do not use
11-Digit NDC Billing Format:
49580029404
NDC to RxNorm Crosswalk:
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG in 20 mL Oral Solution
  • RxCUI: 1020138 - dextromethorphan hydrobromide 1 MG/ML / guaifenesin 20 MG/ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 20 MG / guaifenesin 400 MG per 20 ML Oral Solution
  • RxCUI: 1020138 - dextromethorphan HBr 5 MG / guaifenesin 100 MG per 5 ML Oral Solution
Product Type:
Human Otc Drug
Labeler Name:
P & L Development, Llc
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(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
FDA Application Number:
M012
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
03-26-2021
End Marketing Date:
01-26-2026
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 49580-0294-4?

The NDC Packaged Code 49580-0294-4 is assigned to a package of 1 bottle, plastic in 1 box / 118 ml in 1 bottle, plastic of Mucus Relief Cough Childrens, a human over the counter drug labeled by P & L Development, Llc. The product's dosage form is liquid and is administered via oral form.

Is NDC 49580-0294 included in the NDC Directory?

Yes, Mucus Relief Cough Childrens with product code 49580-0294 is active and included in the NDC Directory. The product was first marketed by P & L Development, Llc on March 26, 2021.

What is the 11-digit format for NDC 49580-0294-4?

The 11-digit format is 49580029404. 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 5-4-1 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
5-4-149580-0294-45-4-249580-0294-04