Mucinex Fast-max Cold And Flu And Mucinex Nightshift Cold And Flu
Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, And Triprolidine Hydrochloride
Rb Health (us) Llc
Human Otc Drug
NDC 63824-137Mucinex Fast-max Cold And Flu And Mucinex Nightshift Cold And Flu also known as Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, And Triprolidine Hydrochloride is a human otc drug labeled by 'Rb Health (us) Llc'. National Drug Code (NDC) number for Mucinex Fast-max Cold And Flu And Mucinex Nightshift Cold And Flu is 63824-137. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Mucinex Fast-max Cold And Flu And Mucinex Nightshift Cold And Flu drug includes . The currest status of Mucinex Fast-max Cold And Flu And Mucinex Nightshift Cold And Flu drug is Active.
Drug Information:
| Drug NDC: | 63824-137 |
| The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC. |
| Proprietary Name: | Mucinex Fast-max Cold And Flu And Mucinex Nightshift Cold And Flu |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. |
| Non Proprietary Name: | Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, Phenylephrine Hydrochloride, And Triprolidine Hydrochloride |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Rb Health (us) Llc |
| Name of Company corresponding to the labeler code segment of the ProductNDC. |
| Dosage Form: | Kit |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. |
| Substance Name: | |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. |
| Route Details: | |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
Marketing Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Marketing Category: | OTC MONOGRAPH FINAL |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (ANDA), BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. |
| Marketing Start Date: | 05 Aug, 2019 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 25 Dec, 2025 |
| This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached. |
| Application Number: | part341 |
| This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null. |
| Listing Expiration Date: | 31 Dec, 2024 |
| This is the date when the listing record will expire if not updated or certified by the firm. |
OpenFDA Information:
An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
| Manufacturer Name: | RB Health (US) LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1116572
2173667
2605573
|
| The RxNorm Concept Unique Identifier. RxCUI is a unique number that describes a semantic concept about the drug product, including its ingredients, strength, and dose forms. |
| Original Packager: | Yes
|
| Whether or not the drug has been repackaged for distribution. |
| UNII: | |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. |
Packaging Information:
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|
| 63824-137-66 | 1 KIT in 1 CARTON (63824-137-66) * 180 mL in 1 BOTTLE (63824-503-66) * 180 mL in 1 BOTTLE (63824-548-66) | 05 Aug, 2019 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. |
Purpose:
Active ingredients (in each 20 ml) mucinex fast-max cold & flu purposes acetaminophen 650 mg pain reliever/fever reducer dextromethorphan hbr 20 mg cough suppressant guaifenesin 400 mg expectorant phenylephrine hcl 10mg nasal decongestant active ingredients (in each 20 ml) mucinex nightshift cold & flu purposes acetaminophen 650 mg pain reliever/fever reducer dextromethorphan hbr 20 mg cough suppressant triprolidine hcl 2.5 mg antihistamine
Product Elements:
Mucinex fast-max cold and flu and mucinex nightshift cold and flu acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride, and triprolidine hydrochloride mucinex nightshift cold and flu acetaminophen, dextromethorphan hydrobromide, and triprolidine hydrochloride ammonium glycyrrhizate anhydrous citric acid ascorbic acid edetate disodium fd&c blue no. 1 fd&c red no. 40 propylene glycol sodium benzoate sorbitol sucralose triacetin triethyl citrate water xanthan gum acetaminophen acetaminophen dextromethorphan hydrobromide dextromethorphan triprolidine hydrochloride triprolidine maximum strength mucinex fast-max cold and flu acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride anhydrous citric acid edetate disodium fd&c blue no. 1 fd&c red no. 40 propyl gallate propylene glycol water sodium benzoate sorbitol sucralose trisodium citrate dihydrate xanthan gum acetaminophen acetaminophen dextromethorphan hydrobromide dextromethorphan guaifenesin guaifenesin phenylephrine hydrochloride phenylephrine
Indications and Usage:
Uses mucinex fast-max cold & flu temporarily relieves these common cold and flu symptoms: cough nasal congestion minor aches and pains sore throat headache stuffy nose sinus congestion and pressure temporarily reduces fever helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive mucinex nightshift cold & flu temporarily relieves these common cold and flu symptoms: cough minor aches and pains sore throat headache runny nose sneezing itching of the nose or throat itchy, watery eyes due to hay fever temporarily reduces fever controls cough to help you get to sleep
Warnings:
Warnings liver warning this product contains acetaminophen. severe liver damage may occur if you take: more than 4000 mg in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 3 or more alcoholic drinks daily while using this product allergy alert acetaminophen may cause severe skin reactions. symptoms may include: skin reddening blisters rash if a skin reaction occurs, stop use and seek medical help right away. sore throat warning if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. do not use with any other drug containing acetaminophen (prescription or nonprescription). if you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are now taking a prescription monoamine oxidase inhibitor (maoi) (certain drugs for depression, psychiatric, or emotional conditions, or parkinson's disease), or for 2 weeks after stoppin
Read more...g the maoi drug. if you do not know if your prescription drug contains an maoi, ask a doctor or pharmacist before taking this product. ask a doctor before use if you have liver disease heart disease (fast-max cold & flu only) diabetes (fast-max cold & flu only) high blood pressure (fast-max cold & flu only) thyroid disease (fast-max cold & flu only) glaucoma (nightshift cold & flu only) trouble urinating due to an enlarged prostate gland a breathing problem such as emphysema or chronic bronchitis (nightshift cold & flu only) persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough that occurs with too much phlegm (mucus) ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin taking sedatives or tranquilizers (nightshift cold & flu only) when using this product do not use more than directed excitability may occur, especially in children (nightshift cold & flu only) marked drowsiness may occur (nightshift cold & flu only) alcohol, sedatives, and tranquilizers may increase drowsiness (nightshift cold & flu only) avoid alcoholic drinks (nightshift cold & flu only) use caution when driving a motor vehicle or operating machinery (nightshift cold & flu only) stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur (fast-max cold & flu only) pain, nasal congestion, or cough gets worse or lasts more than 7 days (fast-max cold & flu only) pain or cough gets worse or lasts more than 7 days (nightshift cold & flu only) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back, or occurs with fever, rash, or headache that lasts. these could be signs of a serious condition. if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children. overdose warning taking more than the recommended dose (overdose) may cause liver damage. in case of overdose, get medical help or contact a poison control center right away. quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
Do Not Use:
Warnings liver warning this product contains acetaminophen. severe liver damage may occur if you take: more than 4000 mg in 24 hours, which is the maximum daily amount with other drugs containing acetaminophen 3 or more alcoholic drinks daily while using this product allergy alert acetaminophen may cause severe skin reactions. symptoms may include: skin reddening blisters rash if a skin reaction occurs, stop use and seek medical help right away. sore throat warning if sore throat is severe, persists for more than 2 days, is accompanied or followed by fever, headache, rash, nausea, or vomiting, consult a doctor promptly. do not use with any other drug containing acetaminophen (prescription or nonprescription). if you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist. if you are now taking a prescription monoamine oxidase inhibitor (maoi) (certain drugs for depression, psychiatric, or emotional conditions, or parkinson's disease), or for 2 weeks after stopping the maoi drug. if you do not know if your prescription drug contains an maoi, ask a doctor or pharmacist before taking this product. ask a doctor before use if you have liver disease heart disease (fast-max cold & flu only) diabetes (fast-max cold & flu only) high blood pressure (fast-max cold & flu only) thyroid disease (fast-max cold & flu only) glaucoma (nightshift cold & flu only) trouble urinating due to an enlarged prostate gland a breathing problem such as emphysema or chronic bronchitis (nightshift cold & flu only) persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or emphysema cough that occurs with too much phlegm (mucus) ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin taking sedatives or tranquilizers (nightshift cold & flu only) when using this product do not use more than directed excitability may occur, especially in children (nightshift cold & flu only) marked drowsiness may occur (nightshift cold & flu only) alcohol, sedatives, and tranquilizers may increase drowsiness (nightshift cold & flu only) avoid alcoholic drinks (nightshift cold & flu only) use caution when driving a motor vehicle or operating machinery (nightshift cold & flu only) stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur (fast-max cold & flu only) pain, nasal congestion, or cough gets worse or lasts more than 7 days (fast-max cold & flu only) pain or cough gets worse or lasts more than 7 days (nightshift cold & flu only) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back, or occurs with fever, rash, or headache that lasts. these could be signs of a serious condition. if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children. overdose warning taking more than the recommended dose (overdose) may cause liver damage. in case of overdose, get medical help or contact a poison control center right away. quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.
When Using:
When using this product do not use more than directed excitability may occur, especially in children (nightshift cold & flu only) marked drowsiness may occur (nightshift cold & flu only) alcohol, sedatives, and tranquilizers may increase drowsiness (nightshift cold & flu only) avoid alcoholic drinks (nightshift cold & flu only) use caution when driving a motor vehicle or operating machinery (nightshift cold & flu only)
Dosage and Administration:
Directions mucinex fast-max cold & flu do not take more than directed (see overdose warning ) do not take more than 6 doses in any 24-hour period measure only with dosing cup provided do not use dosing cup with other products dose as follows or as directed by a doctor adults and children 12 years of age and over: 20 ml in dosing cup provided every 4 hours children under 12 years of age: do not use mucinex nightshift cold & flu do not take more than directed (see overdose warning ) do not take more than 4 doses in any 24-hour period measure only with dosing cup provided do not use dosing cup with other products dose as follows or as directed by a doctor adults and children 12 years of age and over: 20 ml in dosing cup provided every 4 hours children under 12 years of age: do not use
Stop Use:
Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur (fast-max cold & flu only) pain, nasal congestion, or cough gets worse or lasts more than 7 days (fast-max cold & flu only) pain or cough gets worse or lasts more than 7 days (nightshift cold & flu only) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back, or occurs with fever, rash, or headache that lasts. these could be signs of a serious condition.
Package Label Principal Display Panel:
Principal display panel - kit carton ndc 63824-137-66 maximum strength mucinex® fast-max ® cold & flu acetaminophen â pain reliever/fever reducer dextromethorphan hbr â cough suppressant guaifenesin â expectorant ⢠phenylephrine hcl â nasal decongestant sore throat fever headache body pain all in one* chest congestion cough nasal congestion sinus congestion sinus pressure for ages 12+ mucinex® nightshift cold & flu acetaminophen â pain reliever/fever reducer dextromethorphan hbr â cough suppressant triprolidine hcl â antihistamine nighttime relief for a better morning âcough âfever âsore throat ârunny nose âsneezing for ages 12+ three â 6 fl oz (180 ml) bottles total â 18 fl oz (540 ml) principal display panel - kit carton
Further Questions:
Questions? 1-866-mucinex (1-866-682-4639) you may also report side effects to this phone number.