NDC Package 63824-517-01 Mucinex Fast-max Cold, Flu And Sore Throat

Acetaminophen,Guaifenesin,Phenylephrine Hydrochloride,And Dextromethorphan Hydrobromide - 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:
63824-517-01
Package Description:
2 BLISTER PACK in 1 CARTON / 10 TABLET, COATED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Mucinex Fast-max Cold, Flu And Sore Throat
Non-Proprietary Name:
Acetaminophen, Guaifenesin, Phenylephrine Hydrochloride, And Dextromethorphan Hydrobromide
Substance Name:
Acetaminophen; Dextromethorphan Hydrobromide; Guaifenesin; Phenylephrine Hydrochloride
Usage Information:
Do not take more than directed (see Overdose warning)do not take more than 12 caplets in any 24-hour periodadults and children 12 years of age and older: take 2 caplets every 4 hourschildren under 12 years of age: do not use
11-Digit NDC Billing Format:
63824051701
NDC to 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
Product Type:
Human Otc Drug
Labeler Name:
Rb Health (us) Llc
Dosage Form:
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
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:
08-01-2018
End Marketing Date:
09-01-2025
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 63824-517-01?

The NDC Packaged Code 63824-517-01 is assigned to a package of 2 blister pack in 1 carton / 10 tablet, coated in 1 blister pack of Mucinex Fast-max Cold, Flu And Sore Throat, a human over the counter drug labeled by Rb Health (us) Llc. The product's dosage form is tablet, coated and is administered via oral form.

Is NDC 63824-517 included in the NDC Directory?

Yes, Mucinex Fast-max Cold, Flu And Sore Throat with product code 63824-517 is active and included in the NDC Directory. The product was first marketed by Rb Health (us) Llc on August 01, 2018.

What is the 11-digit format for NDC 63824-517-01?

The 11-digit format is 63824051701. 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 5-3-2 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
5-3-263824-517-015-4-263824-0517-01