NDC 68016-879 Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief

Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, And Doxylamine Succinate

NDC Product Code 68016-879

NDC Code: 68016-879

Proprietary Name: Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Acetaminophen, Phenylephrine Hydrochloride, Dextromethorphan Hydrobromide, And Doxylamine Succinate What is the Non-Proprietary Name?
The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.

NDC Code Structure

  • 68016 - Chain Drug Consortium, Llc
    • 68016-879 - Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief

NDC 68016-879-48

Package Description: 1 KIT in 1 PACKAGE * 16 BLISTER PACK in 1 CARTON > 2 CAPSULE in 1 BLISTER PACK * 8 BLISTER PACK in 1 CARTON > 2 CAPSULE in 1 BLISTER PACK

NDC Product Information

Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief with NDC 68016-879 is a a human over the counter drug product labeled by Chain Drug Consortium, Llc. The generic name of Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief is acetaminophen, phenylephrine hydrochloride, dextromethorphan hydrobromide, and doxylamine succinate. The product's dosage form is kit and is administered via form.

Labeler Name: Chain Drug Consortium, Llc

Dosage Form: Kit - A packaged collection of related material.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Inactive Ingredient(s)

About the Inactive Ingredient(s)
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product.

  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
  • GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • FD&C RED NO. 40 (UNII: WZB9127XOA)
  • FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
  • SORBITOL (UNII: 506T60A25R)
  • POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
  • POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • SHELLAC (UNII: 46N107B71O)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
  • D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
  • GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
  • GLYCERIN (UNII: PDC6A3C0OX)
  • FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
  • POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
  • POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
  • PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
  • WATER (UNII: 059QF0KO0R)
  • SHELLAC (UNII: 46N107B71O)
  • SORBITOL (UNII: 506T60A25R)
  • TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Chain Drug Consortium, Llc
Labeler Code: 68016
FDA Application Number: part341 What is the FDA Application Number?
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.

Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/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.

Start Marketing Date: 07-12-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 What is the Listing Expiration Date?
This is the date when the listing record will expire if not updated or certified by the product labeler.

Exclude Flag: N What is the NDC Exclude Flag?
This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA’s requests for correction to deficient or non-compliant submissions. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief Product Label Images

Cold And Flu Multi-symptom Relief/cold And Flu Nighttime Relief Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts - Day Time

Active ingredients (in each capsule) Acetaminophen USP 325 mg Dextromethorphan HBr USP 10 mgPhenylephrine HCl USP 5 mg

Drug Facts - Night Time

Active ingredients (in each capsule) Acetaminophen USP 325 mg Dextromethorphan HBr USP 15 mgDoxylamine succinate USP 6.25 mg

Purpose - Day Time

Pain reliever/fever reducer Cough suppressantNasal decongestant

Purpose - Night Time

Pain reliever/fever reducer Cough suppressantAntihistamine

Uses - Day Time

  • Temporarily relieves common cold/flu symptoms:nasal congestioncough due to minor throat & bronchial irritationsore throatheadacheminor aches & painsfever

Uses - Night Time

  • Temporarily relieves common cold/flu symptoms:nasal congestioncough due to minor throat & bronchial irritationsore throatheadacheminor aches & painsfeverrunny nose & sneezing

Warnings - Day Time

  • Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 4 doses in 24 hrs, which is the maximum daily amount for this product with other drugs containing acetaminophen3 or more alcoholic drinks daily while using this product Sore throat warning: If sore throat is severe, lasts for more than 2 days, occurs with or is followed by fever, headache, rash, nausea, or vomiting, see a doctor promptly.

Warnings - Night Time

  • Liver warning: This product contains acetaminophen. Severe liver damage may occur if you take more than 4 doses in 24 hrs, which is the maximum daily amount for this product with other drugs containing acetaminophen3 or more alcoholic drinks daily while using this product Sore throat warning: If sore throat is severe, lasts for more than 2 days, occurs with or is followed by fever, headache, rash, nausea, or vomiting, see a doctor promptly.

Do Not Use - Day Time

  • 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.

Do Not Use - Night Time

  • 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. to make a child sleep

Ask A Doctor Before Use If You Have - Day Time

  • Liver diseaseheart diseasethyroid diseasediabeteshigh blood pressuretrouble urinating due to enlarged prostate glandcough that occurs with too much phlegm (mucus)persistent or chronic cough as occurs with smoking, asthma, or emphysema

Ask A Doctor Before Use If You Have - Night Time

  • Liver disease glaucomacough that occurs with too much phlegm (mucus)a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema trouble urinating due to enlarged prostate gland

Ask A Doctor Or Pharmacist Before Use If You Are - Day Time

Taking the blood thinning drug warfarin

Ask A Doctor Or Pharmacist Before Use If You Are - Night Time

  • Taking sedatives or tranquilizers taking the blood thinning drug warfarin

When Using This Product,

Do not use more than directed.

When Using This Product - Night Time

  • Do not use more than directedexcitability may occur, especially in children marked drowsiness may occur avoid alcoholic drinks be careful when driving a motor vehicle or operating machinery alcohol, sedatives, & tranquilizers may increase drowsiness

Stop Use And Ask A Doctor If - Day Time

  • You get nervous, dizzy or sleeplesssymptoms get worse or last more than 5 days (children) or 7 days (adults)fever gets worse or lasts more than 3 daysredness or swelling is presentnew symptoms occurcough comes back, or occurs with rash or headache that lasts.These could be signs of a serious condition.

Stop Use And Ask A Doctor If - Night Time

  • Pain or cough gets worse or lasts more than 7 days fever gets worse or lasts more than 3 daysredness 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.

If Pregnant Or Breast-Feeding, - Night Time

Ask a health professional before use.

Keep Out Of Reach Of Children. - Day Time

Overdose warning:Taking more than directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults & for children even if you do not notice any signs or symptoms.

Keep Out Of Reach Of Children. - Night Time

Overdose warning:Taking more than directed can cause serious health problems. In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222). Quick medical attention is critical for adults & for children even if you do not notice any signs or symptoms.

Directions - Day Time

  • Take only as directed – see Overdose warningdo not exceed 4 doses per 24 hoursadults & children 12 yrs & over 2 capsules with water every 4 hrs children 4 to under 12 yrs ask a doctor children under 4 yrs do not use when using other Daytime or Nighttime products, carefully read each label to ensure correct dosing

Directions - Night Time

  • Take only as directed – see Overdose warningdo not exceed 4 doses per 24 hoursadults & children 12 yrs & over 2 capsules with water every 6 hrs children 4 to under 12 yrs ask a doctor children under 4 yrs do not use when using other Daytime or Nighttime products, carefully read each label to ensure correct dosing

Other Information - Day Time

  • Store at room temperature

Other Information - Night Time

  • Store at room temperature

Inactive Ingredients - Day Time

Citric acid anhydrous, gelatin, glycerin, Neelicert FD & C Red No. 40, Neelicert FD & C Yellow No. 6, noncrystallizing sorbitol solution, polyethylene glycol, povidone, propylene glycol, purified water, shellac glaze, titanium dioxide

Inactive Ingredients - Night Time

D&C Yellow No. 10, gelatin, glycerin, Neelicert FD&C Blue No. 1, polyethylene glycol, povidone, propylene glycol, purified water, shellac glaze, sorbitol sorbitan solution, titanium dioxide

* Please review the disclaimer below.

Previous Code
68016-878
Next Code
68016-939