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NDC 63824-0118-66 Mucinex Fast-Max DM Max and Mucinex Nightshift Cold and Flu Details
Mucinex Fast-Max DM Max and Mucinex Nightshift Cold and Flu
Mucinex Fast-Max DM Max and Mucinex Nightshift Cold and Flu is a KIT in the HUMAN OTC DRUG category. It is labeled and distributed by RB Health (US) LLC. The primary component is .
MedlinePlus Drug Summary
Dextromethorphan is used to temporarily relieve cough caused by the common cold, the flu, or other conditions. Dextromethorphan will relieve a cough but will not treat the cause of the cough or speed recovery. Dextromethorphan is in a class of medications called antitussives. It works by decreasing activity in the part of the brain that causes coughing.
Related Packages: 63824-0118-66Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Dextromethorphan
Guaifenesin is used to relieve chest congestion. Guaifenesin may help control symptoms but does not treat the cause of symptoms or speed recovery. Guaifenesin is in a class of medications called expectorants. It works by thinning the mucus in the air passages to make it easier to cough up the mucus and clear the airways.
Related Packages: 63824-0118-66Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Guaifenesin
Product Information
| NDC | 63824-0118 |
|---|---|
| Product ID | 63824-118_fda3d836-0038-ee77-e053-6394a90ac66b |
| Associated GPIs | 4399850450C410 |
| GCN Sequence Number | 081041 |
| GCN Sequence Number Description | triprolidine/DM/acetaminoph/GG LIQUID SEQ 2.5-650/20 ORAL |
| HIC3 | B4V |
| HIC3 Description | ANTITUSSIVE-1ST GEN ANTST-ANALGESIC-EXPECT COMB |
| GCN | 48044 |
| HICL Sequence Number | 046532 |
| HICL Sequence Number Description | TRIPROLIDINE HCL/DEXTROMETHORPHAN/ACETAMINOPHEN/GUAIFENESIN |
| Brand/Generic | Brand |
| Proprietary Name | Mucinex Fast-Max DM Max and Mucinex Nightshift Cold and Flu |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Triprolidine Hydrochloride |
| Product Type | HUMAN OTC DRUG |
| Dosage Form | KIT |
| Route | n/a |
| Active Ingredient Strength | n/a |
| Active Ingredient Units | n/a |
| Substance Name | n/a |
| Labeler Name | RB Health (US) LLC |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | OTC MONOGRAPH FINAL |
| Application Number | part341 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 63824-0118-66 (63824011866)
| NDC Package Code | 63824-118-66 |
|---|---|
| Billing NDC | 63824011866 |
| Package | 1 KIT in 1 CARTON (63824-118-66) * 180 mL in 1 BOTTLE (63824-503-66) * 180 mL in 1 BOTTLE (63824-019-66) |
| Marketing Start Date | 2022-06-30 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |