Nighttime Cold And Flu Capsule, Liquid Filled (acetaminophen 325mg, Dextromethorpha Hbr 15mg And Doxylamine Succinate 6.25mg)

Nighttime Cold And Flu Capsule, Liquid Filled (acetaminophen 325mg, Dextromethorpha Hbr 15mg And Doxylamine Succinate 6.25mg)
SPL v2
SPL
SPL Set ID 13a3a043-82c1-4f78-89a7-0b03af65b9fd
Route
ORAL
Published
Effective Date 2021-03-02
Document Type 34390-5 HUMAN OTC DRUG LABEL

Drug Facts

Composition & Product

Active Ingredients
Acetaminophen (325 mg) Dextromethorphan (15 mg) Doxylamine (6.25 mg)
Inactive Ingredients
Polyethylene Glycol 400 Propylene Glycol Povidone K30 Fd&c Blue No. 1 D&c Yellow No. 10 Titanium Dioxide Gelatin Glycerin Sorbitol Water

Identifiers & Packaging

Marketing Status
OTC MONOGRAPH FINAL Active Since 2021-03-01

Description

Acetaminophen 325 mg Dextromethorphan HBr 15 mg Doxylamine Succinate 6.25 mg

Purpose

Pain reliever/ fever reducer Cough suppressant Antihistamine


Medication Information

Purpose

Pain reliever/ fever reducer Cough suppressant Antihistamine

Description

Acetaminophen 325 mg Dextromethorphan HBr 15 mg Doxylamine Succinate 6.25 mg

Uses:

temporarily relieves common cold/flu symptoms:

  • cough due to minor throat & bronchial irritation
  • sore throat
  • headache
  • minor aches/pains
  • fever
  • runny nose & sneezing
Purpose:

Pain reliever/ fever reducer

Cough suppressant

Antihistamine

Warnings:

Liver warning This product contains acetaminophen. Severe liver damage may occur if you take:

  • more than 4 doses in 24 hours, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product

Sore throat warning  If sore throat is severe, lasts more than 2 days, occurs with or is followed by fever, headache, rash, nausea, or vomiting, see a doctor promptly.

Directions
  • take only as directed - see Overdose warning
  • do not exceed 4 doses per 24 hours
Adults and children 12 years of age and older 2 LiquiCaps with water every 4 hours
Children under 12 years of age ask doctor

When using other Nighttime or Daytime products, carefully read each label to ensure correct dosing.

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.
  • To make a child sleep
Other Information
  • store at room temperature 59°-86°F (15°-30°C)
Inactive Ingredients

polyethylene glycol 400, propylene glycol, povidone k30, fd&c blue no. 1, d&c yellow no. 10, titanium dioxide, gelatin, glycerin, sorbitol, water

When Using This Product

do not use more than directed

excitability may occur, especially in children

marked drowsiness may occur

avoid alcoholic drinks

be careful when driving a motor vehicle or operating machinery

alcohol, sedatives, and tranquilizers may increase drowsiness

Stop Use and Ask A Doctor If
  • pain or cough gets worse or lasts more than 7 days
  • 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.
Ask A Doctor Before Use If You Have
  • liver disease
  • glaucoma
  • cough 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
Active Ingredients (in Each Capsule)

Acetaminophen 325 mg

Dextromethorphan HBr 15 mg

Doxylamine Succinate 6.25 mg

Principal Display Panel Shipping Label

Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate capsules

Each Softgel Contains:

(Acetaminophen USP 325 mg, Dextromethorphan Hydrobromide USP 15 mg, Doxylamine Succinate 6.25 mg)

LOT NO:

DRUM NO:

MFG DATE:

QUANTITY:

NDC NO: 55629-014-

EXP DATE:

WARNING:

KEEP OUT OF REACH OF CHILDREN

STORE CONTROLLED ROOM TEMPERATURE OF 59° - 86°F (15° - 30°C)

PROTECT FROM LIGHT, MOISTURE AND FREEZING

THIS IS A BULK SHIPMENT INTENDED FOR FURTHER PROCESSING ONLY.

CONTENTS SHOULD BE APPROVED, REPACKAGED IMMEDIATELY AND LABELED IN STRICT CONFORMANCE WITH

THE F.D & C.ACT AND REGULATIONS THEREUNDER.


Structured Label Content

Uses:

temporarily relieves common cold/flu symptoms:

  • cough due to minor throat & bronchial irritation
  • sore throat
  • headache
  • minor aches/pains
  • fever
  • runny nose & sneezing
Purpose:

Pain reliever/ fever reducer

Cough suppressant

Antihistamine

Warnings:

Liver warning This product contains acetaminophen. Severe liver damage may occur if you take:

  • more than 4 doses in 24 hours, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product

Sore throat warning  If sore throat is severe, lasts more than 2 days, occurs with or is followed by fever, headache, rash, nausea, or vomiting, see a doctor promptly.

Directions
  • take only as directed - see Overdose warning
  • do not exceed 4 doses per 24 hours
Adults and children 12 years of age and older 2 LiquiCaps with water every 4 hours
Children under 12 years of age ask doctor

When using other Nighttime or Daytime products, carefully read each label to ensure correct dosing.

Do Not Use (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.
  • To make a child sleep
Other Information
  • store at room temperature 59°-86°F (15°-30°C)
Inactive Ingredients (Inactive ingredients)

polyethylene glycol 400, propylene glycol, povidone k30, fd&c blue no. 1, d&c yellow no. 10, titanium dioxide, gelatin, glycerin, sorbitol, water

When Using This Product (When using this product)

do not use more than directed

excitability may occur, especially in children

marked drowsiness may occur

avoid alcoholic drinks

be careful when driving a motor vehicle or operating machinery

alcohol, sedatives, and tranquilizers may increase drowsiness

Stop Use and Ask A Doctor If (Stop use and ask a doctor if)
  • pain or cough gets worse or lasts more than 7 days
  • 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.
Ask A Doctor Before Use If You Have (Ask a doctor before use if you have)
  • liver disease
  • glaucoma
  • cough 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
Active Ingredients (in Each Capsule) (Active ingredients (in each capsule))

Acetaminophen 325 mg

Dextromethorphan HBr 15 mg

Doxylamine Succinate 6.25 mg

Principal Display Panel Shipping Label (PRINCIPAL DISPLAY PANEL - Shipping Label)

Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate capsules

Each Softgel Contains:

(Acetaminophen USP 325 mg, Dextromethorphan Hydrobromide USP 15 mg, Doxylamine Succinate 6.25 mg)

LOT NO:

DRUM NO:

MFG DATE:

QUANTITY:

NDC NO: 55629-014-

EXP DATE:

WARNING:

KEEP OUT OF REACH OF CHILDREN

STORE CONTROLLED ROOM TEMPERATURE OF 59° - 86°F (15° - 30°C)

PROTECT FROM LIGHT, MOISTURE AND FREEZING

THIS IS A BULK SHIPMENT INTENDED FOR FURTHER PROCESSING ONLY.

CONTENTS SHOULD BE APPROVED, REPACKAGED IMMEDIATELY AND LABELED IN STRICT CONFORMANCE WITH

THE F.D & C.ACT AND REGULATIONS THEREUNDER.


Advanced Ingredient Data


Raw Label Data

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