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Cold and Flu Daytime by Lil' Drug Store Products, Inc

Dosage form: capsule, liquid filled
Ingredients: Acetaminophen 325mg, Dextromethorphan Hydrobromide 10mg, Phenylephrine Hydrochloride 5mg
Labeler: Lil' Drug Store Products, Inc
NDC Code: 66715-6831

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Cold & Flu Daytime

Drug Facts

Active ingredients (in each softgel)Purpose
Acetaminophen 325 mgPain reliever/fever reducer
Dextromethorphan HBr 10 mgCough suppressant
Phenylephrine HCl 5 mgNasal decongestant

Uses

temporarily relieves common cold and flu symptoms:

  • minor aches and pains
  • headache
  • sore throat
  • nasal congestion
  • fever
  • cough due to minor throat and bronchial irritation

Warnings

Liver warning

This product contains 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 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
  • diabetes
  • heart disease
  • thyroid disease
  • high blood pressure
  • trouble urinating due to an enlarged prostate gland
  • persistent or chronic cough such as occurs with smoking, asthma, 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

When using this product, do not exceed recommended dosage.

Stop use and ask a doctor if
  • pain, cough, or nasal congestion gets worse or lasts more than 7 days
  • new symptoms occur
  • nervousness, dizziness, or sleeplessness occur
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • 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.

Directions
  • do not take more than directed (see Overdose warning)
  • do not take more than 4 doses in 24 hours
  • adults and children 12 years and over: take 2 softgels with water every 4 hours
  • swallow whole; do not crush, chew, or dissolve
  • children under 12 years: do not use
  • when using other Daytime or Nighttime products, carefully read each label to ensure correct dosing

Other information
  • store at room temperature 15°- 30°C (59°- 86°F)
  • avoid excessive heat

Inactive ingredients

butylated hydroxyanisole, butylated hydroxytouluene, carminic acid1, edible white ink, D&C yellow #101, FD&C red #40, D&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sodium metabisulfite1, sorbitan, sorbitol


may contain this ingredient

Questions?

call toll-free 1-877-507-6516 (M-F 8AM-4:30PM CST)

Distributed by:
Lil' Drug Store Products, Inc.
1201 Continental Pl NE
Cedar Rapids, IA 52402

PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC 66715-6831

QUALITY
⋆ GUARANTEED ⋆

Compare to the Active Ingredients in
Vicks® DayQuil® LiquiCaps®**

Cold & Flu
Daytime

Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

Relieves
• Aches • Fever
• Sore Throat • Cough
• Nasal Congestion

ACTUAL SIZE

12
Softgels

Lil'
Drug Store®

PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC 66715-6851

QUALITY
⋆ GUARANTEED ⋆

Compare to the Active Ingredients in
Vicks® DayQuil® LiquiCaps®**

Cold & Flu
Daytime

Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

Relieves
• Aches • Fever
• Sore Throat • Cough
• Nasal Congestion

ACTUAL SIZE

12
Softgels

Lil'
Drug Store®

PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC 66715-6852

QUALITY
⋆ GUARANTEED ⋆

Compare to the Active Ingredients in
Vicks® DayQuil® LiquiCaps®**

Cold & Flu
Daytime

Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

Relieves
• Aches • Fever
• Sore Throat • Cough
• Nasal Congestion

ACTUAL SIZE

12
Softgels

Lil'
Drug Store®

PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC 66715-6853

QUALITY
⋆ GUARANTEED ⋆

Compare to the Active Ingredients in
Vicks® DayQuil® LiquiCaps®**

Cold & Flu
Daytime

Acetaminophen, Dextromethorphan HBr, and Phenylephrine HCl
Pain Reliever/Fever Reducer, Cough Suppressant, Nasal Decongestant

Relieves
• Aches • Fever
• Sore Throat • Cough
• Nasal Congestion

ACTUAL SIZE

12
Softgels

Lil'
Drug Store®

COLD AND FLU DAYTIME 
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6831
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (Acetaminophen) Acetaminophen325 mg
Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide10 mg
Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride5 mg
Inactive Ingredients
Ingredient NameStrength
Butylated Hydroxyanisole 
Butylated Hydroxytoluene 
Carminic Acid 
FD&C red No. 40 
FD&C yellow No. 6 
D&C yellow No. 10 
GELATIN, UNSPECIFIED 
Glycerin 
Polyethylene Glycol, Unspecified 
Povidone, Unspecified 
Propylene Glycol 
Sodium Metabisulfite 
Sorbitan 
Sorbitol 
Water 
Product Characteristics
ColorORANGEScoreno score
ShapeOVALSize20mm
FlavorImprint Code95A
Contains    
Packaging
#Item CodePackage Description
1NDC:66715-6831-06 BLISTER PACK in 1 CARTON
12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34109/05/2014
COLD AND FLU DAYTIME 
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6851
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (Acetaminophen) Acetaminophen325 mg
Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide10 mg
Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride5 mg
Inactive Ingredients
Ingredient NameStrength
Butylated Hydroxyanisole 
Butylated Hydroxytoluene 
Carminic Acid 
FD&C red No. 40 
FD&C yellow No. 6 
D&C yellow No. 10 
GELATIN, UNSPECIFIED 
Glycerin 
Polyethylene Glycol, Unspecified 
Povidone, Unspecified 
Propylene Glycol 
Sodium Metabisulfite 
Sorbitan 
Sorbitol 
Water 
Product Characteristics
ColorORANGEScoreno score
ShapeOVALSize20mm
FlavorImprint CodeP19
Contains    
Packaging
#Item CodePackage Description
1NDC:66715-6851-06 BLISTER PACK in 1 CARTON
12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34109/05/2014
COLD AND FLU DAYTIME 
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6852
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (Acetaminophen) Acetaminophen325 mg
Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide10 mg
Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride5 mg
Inactive Ingredients
Ingredient NameStrength
Butylated Hydroxyanisole 
Butylated Hydroxytoluene 
Carminic Acid 
FD&C red No. 40 
FD&C yellow No. 6 
D&C yellow No. 10 
GELATIN, UNSPECIFIED 
Glycerin 
Polyethylene Glycol, Unspecified 
Povidone, Unspecified 
Propylene Glycol 
Sodium Metabisulfite 
Sorbitan 
Sorbitol 
Water 
Product Characteristics
ColorORANGEScoreno score
ShapeOVALSize20mm
FlavorImprint Code512
Contains    
Packaging
#Item CodePackage Description
1NDC:66715-6852-06 BLISTER PACK in 1 CARTON
12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34109/05/2014
COLD AND FLU DAYTIME 
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66715-6853
Route of AdministrationORALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (Acetaminophen) Acetaminophen325 mg
Dextromethorphan Hydrobromide (Dextromethorphan) Dextromethorphan Hydrobromide10 mg
Phenylephrine Hydrochloride (Phenylephrine) Phenylephrine Hydrochloride5 mg
Inactive Ingredients
Ingredient NameStrength
Butylated Hydroxyanisole 
Butylated Hydroxytoluene 
Carminic Acid 
FD&C red No. 40 
FD&C yellow No. 6 
D&C yellow No. 10 
GELATIN, UNSPECIFIED 
Glycerin 
Polyethylene Glycol, Unspecified 
Povidone, Unspecified 
Propylene Glycol 
Sodium Metabisulfite 
Sorbitan 
Sorbitol 
Water 
Product Characteristics
ColorORANGEScoreno score
ShapeOVALSize20mm
FlavorImprint CodeP119
Contains    
Packaging
#Item CodePackage Description
1NDC:66715-6853-06 BLISTER PACK in 1 CARTON
12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart34109/05/2014
Labeler - Lil' Drug Store Products, Inc (093103646)

 
Lil' Drug Store Products, Inc

← See all Cold and Flu Daytime brands

Medically reviewed on Dec 26, 2017

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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