Cold And Flu Relief Multi Symptom
Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Doxylamine Succinate
Winco Foods, Llc
Human Otc Drug
NDC 67091-309Cold And Flu Relief Multi Symptom also known as Acetaminophen, Dextromethorphan Hbr, Phenylephrine Hcl, Doxylamine Succinate is a human otc drug labeled by 'Winco Foods, Llc'. National Drug Code (NDC) number for Cold And Flu Relief Multi Symptom is 67091-309. This drug is available in dosage form of Kit. The names of the active, medicinal ingredients in Cold And Flu Relief Multi Symptom drug includes . The currest status of Cold And Flu Relief Multi Symptom drug is Active.
Drug Information:
| Drug NDC: | 67091-309 |
| 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: | Cold And Flu Relief Multi Symptom |
| Also known as the trade name. It is the name of the product chosen by the labeler. |
| Proprietary Name Base: | Cold And Flu Relief |
| The base of the Brand/Proprietary name excluding its suffix. |
| Proprietary Name Suffix: | Multi symptom |
| A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard. |
| 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 Hbr, Phenylephrine Hcl, Doxylamine Succinate |
| Also known as the generic name, this is usually the active ingredient(s) of the product. |
| Labeler Name: | Winco Foods, 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: | ORAL
|
| 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: | 30 Sep, 2016 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. |
| Marketing End Date: | 16 Jan, 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, 2023 |
| 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: | WinCo Foods, LLC
|
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. |
| RxCUI: | 1086997
1094549
1311150
|
| 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. |
| UPC: | 0070552241213
|
| UPC stands for Universal Product Code. |
| 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 |
|---|
| 67091-309-48 | 1 KIT in 1 CARTON (67091-309-48) * 16 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK * 32 BLISTER PACK in 1 CARTON / 1 CAPSULE in 1 BLISTER PACK | 30 Sep, 2016 | 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:
Purpose for daytime pain reliever/fever reducer cough suppressant nasal decongestant
Purpose for nighttime pain reliever/fever reducer cough suppressant antihistamine
Product Elements:
Cold and flu relief multi symptom acetaminophen, dextromethorphan hbr, phenylephrine hcl, doxylamine succinate cold and flu relief multi symptom nighttime acetaminophen, dextromethorphan hydrobromide, doxylamine succinate acetaminophen acetaminophen dextromethorphan hydrobromide dextromethorphan doxylamine succinate doxylamine d&c yellow no. 10 fd&c blue no. 1 gelatin glycerin polyethylene glycol, unspecified povidone propylene glycol water sorbitan sorbitol p30;94a;215;p120 cold and flu relief multi symptom non drowsy daytime acetaminophen, dextromethorphan hbr, phenylephrine hcl acetaminophen acetaminophen dextromethorphan hydrobromide dextromethorphan phenylephrine hydrochloride phenylephrine butylated hydroxyanisole butylated hydroxytoluene fd&c red no. 40 fd&c yellow no. 6 gelatin glycerin polyethylene glycol, unspecified povidone propylene glycol water sorbitan sorbitol carminic acid d&c yellow no. 10 sodium metabisulfite p19;95a;512;p119
Indications and Usage:
Uses temporarily relieves common cold and flu symptoms: sore throat headache minor aches and pains fever cough due to minor throat and bronchial irritation nasal congestion (daytime only) runny nose and sneezing (nighttime only)
Warnings:
Warnings liver warning: these products contain acetaminophen. severe liver damage may occur if you take: more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day 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 parkinsons disease), or for 2 weeks after stopping the m
Read more...aoi 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 (daytime-nighttime) heart disease (daytime) diabetes (daytime) thyroid disease (daytime) high blood pressure (daytime) glaucoma (nighttime) cough that occurs with too much phlegm (mucus) trouble urinating due to an enlarged prostate gland persistent or chronic cough such as occurs with smoking, asthma, emphysema (daytime) a breathing problem or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema (nighttime) ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin taking sedatives or tranquilizers (nighttime only) when using this product, daytime: do not use more than directed. nighttime: excitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur (daytime only) pain, cough, and nasal congestion gets worse or lasts more than 7 days (daytime) pain or cough gets worse or lasts more than 3 days (nighttime) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back or occurs with 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 can 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: these products contain acetaminophen. severe liver damage may occur if you take: more than 4,000 mg of acetaminophen in 24 hours with other drugs containing acetaminophen 3 or more alcoholic drinks every day 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 parkinsons 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 (daytime-nighttime) heart disease (daytime) diabetes (daytime) thyroid disease (daytime) high blood pressure (daytime) glaucoma (nighttime) cough that occurs with too much phlegm (mucus) trouble urinating due to an enlarged prostate gland persistent or chronic cough such as occurs with smoking, asthma, emphysema (daytime) a breathing problem or chronic cough such as occurs with smoking, asthma, chronic bronchitis or emphysema (nighttime) ask a doctor or pharmacist before use if you are taking the blood thinning drug warfarin taking sedatives or tranquilizers (nighttime only) when using this product, daytime: do not use more than directed. nighttime: excitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur (daytime only) pain, cough, and nasal congestion gets worse or lasts more than 7 days (daytime) pain or cough gets worse or lasts more than 3 days (nighttime) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back or occurs with 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 can 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, daytime: do not use more than directed. nighttime: excitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks alcohol, sedatives, and tranquilizers may increase drowsiness be careful when driving a motor vehicle or operating machinery
Dosage and Administration:
Directions do not take more than directed (see overdose warning ) do not take more than 4 doses in 24 hours swallow whole; do not crush, chew, or dissolve daytime : adults and children 12 years and over: take 2 softgels with water every 4 hours nighttime : adults and children 12 years and over: take 2 softgels with water every 6 hours children under 12 years: do not use
Stop Use:
Stop use and ask a doctor if nervousness, dizziness, or sleeplessness occur (daytime only) pain, cough, and nasal congestion gets worse or lasts more than 7 days (daytime) pain or cough gets worse or lasts more than 3 days (nighttime) fever gets worse or lasts more than 3 days redness or swelling is present new symptoms occur cough comes back or occurs with rash or headache that lasts these could be signs of a serious condition.
Package Label Principal Display Panel:
Principal display panel ** compare to the active ingredients in vicks® dayquil® & nyquil® liquicaps® multi-symptom cold & flu relief non-drowsy daytime acetaminophen / pain reliever - fever reducer dextromethorphan hbr / cough suppressant phenylephrine hci / nasal decongestant relieves: aches, fever, sore throat, cough & nasal congestion nighttime acetaminophen / pain reliever - fever reducer dextromethorphan hbr / cough suppressant doxylamine succinate / antihistamine relieves: aches, fever, sore throat, cough, sneezing & runny nose. softgels **liquid filled capsules when using daytime and nighttime products, carefully read the labeling to ensure correct dosing. keep outer carton for complete warnings and product information tamper evident: do not use if carton is opened or if blister unit is torn, broken or shows any signs of tampering. this product is not manufactured or distributed by the procter & gamble company, vicks®, dayquil®, nyquil® and liquicap® are registered trademarks of the procter & gamble company. distributed by: winco foods, llc boise, id 83704 www.wincofoods.com
Product label winco foods daytime nighttime multi-symptom cold & flu relief acetaminophen 325 mg, dextromethorphan hbr 10 mg, phenylephrine hci 5 mg dextromethorphan hbr 15 mg, doxylamine succinate 6.25 mg
Further Questions:
Questions or comments? or to report an adverse event call 800-824-1706 monday-friday 9am-4pm mst