NDC Package 68210-1390-1 Mucus Relief Dm

Guaifenesin And Dextromethorphan Hydrobromide Capsule, Liquid Filled Oral - 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:
68210-1390-1
Package Description:
1 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product Code:
Proprietary Name:
Mucus Relief Dm
Non-Proprietary Name:
Guaifenesin And Dextromethorphan Hydrobromide
Substance Name:
Dextromethorphan Hydrobromide; Guaifenesin
Usage Information:
Adults and children 12 years of age and older:Take with a full glass of water.Take 1 softgel every 4 hours with a full glass of water while symptoms persist. Do not exceed 6 doses in 24 hours.Children under 12 years of age: do not use
11-Digit NDC Billing Format:
68210139001
NDC to RxNorm Crosswalk:
  • RxCUI: 1661740 - dextromethorphan HBr 20 MG / guaiFENesin 400 MG Oral Capsule
  • RxCUI: 1661740 - dextromethorphan hydrobromide 20 MG / guaifenesin 400 MG Oral Capsule
Product Type:
Human Otc Drug
Labeler Name:
Spirit Pharmaceuticals Llc
Dosage Form:
Capsule, Liquid Filled - A solid dosage form in which the drug is enclosed within a soluble, gelatin shell which is plasticized by the addition of a polyol, such as sorbitol or glycerin, and is therefore of a somewhat thicker consistency than that of a hard shell capsule; typically, the active ingredients are dissolved or suspended in a liquid vehicle.
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:
03-17-2020
Listing Expiration Date:
12-31-2025
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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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68210-1390-44 BLISTER PACK in 1 CARTON / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68210-1390-1?

The NDC Packaged Code 68210-1390-1 is assigned to a package of 1 blister pack in 1 carton / 10 capsule, liquid filled in 1 blister pack of Mucus Relief Dm, a human over the counter drug labeled by Spirit Pharmaceuticals Llc. The product's dosage form is capsule, liquid filled and is administered via oral form.

Is NDC 68210-1390 included in the NDC Directory?

Yes, Mucus Relief Dm with product code 68210-1390 is active and included in the NDC Directory. The product was first marketed by Spirit Pharmaceuticals Llc on March 17, 2020 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 68210-1390-1?

The 11-digit format is 68210139001. 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
5-4-168210-1390-15-4-268210-1390-01