COLD AND FLU DAYTIME- acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled
Lil' Drug Store Products, Inc

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)	Purposes
Acetaminophen 325 mg	Pain reliever/fever reducer
Dextromethorphan HBr 10 mg	Cough suppressant
Phenylephrine HCl 5 mg	Nasal 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 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 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
nervousness, dizziness, or sleeplessness occur
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.

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 between 15°-30°C (59°-86°F)
avoid excessive heat

Inactive ingredients

butylated hydroxyanisole1, butylated hydroxytoluene1, FD&C red #401, FD&C yellow #6, gelatin, glycerin, polyethylene glycol, povidone, propylene glycol, purified water, sorbitan, sorbitol, titanium dioxide1, white ink

1: contains one or more of these ingredients

Questions or comments?

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

Distributed by:
Lil' Drug Store Products, Inc.
9300 Earhart Lane SW
Cedar Rapids, IA 52404

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

QUALITY
⋆ GUARANTEED ⋆

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

Non-drowsy

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 66715-6831

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

QUALITY
⋆ GUARANTEED ⋆

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

Non-drowsy

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

PRINCIPAL DISPLAY PANEL - 12 Softgel Blister Pack Carton - NDC 66715-6951

QUALITY
⋆ GUARANTEED ⋆

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

Non-drowsy

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 66715-6951

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 66715-6852

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®

Principal Display Panel - 12 Softgel Blister Pack Carton - NDC 66715-6853

COLD AND FLU DAYTIME
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66715-6831
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	325 mg
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV)	Phenylephrine Hydrochloride	5 mg

Ingredient Name	Strength
Inactive Ingredients
Butylated Hydroxyanisole (UNII: REK4960K2U)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
FD&C red No. 40 (UNII: WZB9127XOA)
FD&C yellow No. 6 (UNII: H77VEI93A8)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
Glycerin (UNII: PDC6A3C0OX)
Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)
Povidone, Unspecified (UNII: FZ989GH94E)
Propylene Glycol (UNII: 6DC9Q167V3)
Sorbitan (UNII: 6O92ICV9RU)
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	ORANGE	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	95A
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66715-6831-0	6 in 1 CARTON	10/01/2015	02/21/2023
1		2 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part341	09/05/2014	02/21/2023

COLD AND FLU DAYTIME
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66715-6851
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	325 mg
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV)	Phenylephrine Hydrochloride	5 mg

Ingredient Name	Strength
Inactive Ingredients
Butylated Hydroxyanisole (UNII: REK4960K2U)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
FD&C red No. 40 (UNII: WZB9127XOA)
FD&C yellow No. 6 (UNII: H77VEI93A8)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
Glycerin (UNII: PDC6A3C0OX)
Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)
Povidone, Unspecified (UNII: FZ989GH94E)
Propylene Glycol (UNII: 6DC9Q167V3)
Sorbitan (UNII: 6O92ICV9RU)
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	ORANGE	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	P19
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66715-6851-0	6 in 1 CARTON	10/01/2015	02/21/2023
1		2 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part341	09/05/2014	02/21/2023

COLD AND FLU DAYTIME
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66715-6951
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	325 mg
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg

Ingredient Name	Strength
Inactive Ingredients
Butylated Hydroxyanisole (UNII: REK4960K2U)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
FD&C Red No. 40 (UNII: WZB9127XOA)
FD&C Yellow No. 6 (UNII: H77VEI93A8)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
Glycerin (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
Propylene Glycol (UNII: 6DC9Q167V3)
Water (UNII: 059QF0KO0R)
Sorbitan (UNII: 6O92ICV9RU)
Sorbitol (UNII: 506T60A25R)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	ORANGE	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	AS016
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66715-6951-0	6 in 1 CARTON	01/28/2019	02/21/2023
1		2 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC monograph final	part341	09/05/2014	02/21/2023

COLD AND FLU DAYTIME
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66715-6852
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	325 mg
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV)	Phenylephrine Hydrochloride	5 mg

Ingredient Name	Strength
Inactive Ingredients
Butylated Hydroxyanisole (UNII: REK4960K2U)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
FD&C red No. 40 (UNII: WZB9127XOA)
FD&C yellow No. 6 (UNII: H77VEI93A8)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
Glycerin (UNII: PDC6A3C0OX)
Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)
Povidone, Unspecified (UNII: FZ989GH94E)
Propylene Glycol (UNII: 6DC9Q167V3)
Sorbitan (UNII: 6O92ICV9RU)
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	ORANGE	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	512
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66715-6852-0	6 in 1 CARTON	10/01/2015	01/28/2022
1		2 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part341	09/05/2014	01/28/2022

COLD AND FLU DAYTIME
acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride capsule, liquid filled

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:66715-6853
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D)	Acetaminophen	325 mg
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS)	Dextromethorphan Hydrobromide	10 mg
Phenylephrine Hydrochloride (UNII: 04JA59TNSJ) (Phenylephrine - UNII:1WS297W6MV)	Phenylephrine Hydrochloride	5 mg

Ingredient Name	Strength
Inactive Ingredients
Butylated Hydroxyanisole (UNII: REK4960K2U)
Butylated Hydroxytoluene (UNII: 1P9D0Z171K)
FD&C red No. 40 (UNII: WZB9127XOA)
FD&C yellow No. 6 (UNII: H77VEI93A8)
GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
Glycerin (UNII: PDC6A3C0OX)
Polyethylene Glycol, Unspecified (UNII: 3WJQ0SDW1A)
Povidone, Unspecified (UNII: FZ989GH94E)
Propylene Glycol (UNII: 6DC9Q167V3)
Sorbitan (UNII: 6O92ICV9RU)
Sorbitol (UNII: 506T60A25R)
Water (UNII: 059QF0KO0R)
Titanium Dioxide (UNII: 15FIX9V2JP)

Product Characteristics
Color	ORANGE	Score	no score
Shape	OVAL	Size	20mm
Flavor		Imprint Code	P119
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:66715-6853-0	6 in 1 CARTON	10/01/2015	01/28/2022
1		2 in 1 BLISTER PACK; Type 0: Not a Combination Product

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
OTC MONOGRAPH FINAL	part341	09/05/2014	01/28/2022

Labeler - Lil' Drug Store Products, Inc (093103646)

Revised: 10/2020

Document Id: 63eb39c3-60c0-47f6-a7c4-ce8cfa4394c2

Set id: b9cf59e7-e298-46a2-a3a0-abf23f8678f3

Version: 7

Effective Time: 20201009

Lil' Drug Store Products, Inc