TARGET MAXIMUM STRENGTH COLD FLU AND SORE THROAT OVERNIGHT COLD AND FLU- acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and triprolidine hcl 
TARGET CORPORATION

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Maximum Strength Cold, Flu & Sore Throat and Overnight Cold & Flu Value Pack

Drug Facts

Active ingredients (in each 20 mL)
MAXIMUM STRENGTH COLD, FLU & SORE THROAT
Purposes

Acetaminophen 650 mg

Dextromethorphan HBr 20 mg

Pain reliever/fever reducer

Cough suppressant

Guaifenesin 400 mg

Phenylephrine HCl 10 mg

Expectorant

Nasal decongestant

Active ingredients (in each 20 mL)Purposes
MAXIMUM STRENGTH OVERNIGHT COLD & FLU

Acetaminophen 650 mg

Pain reliever/fever reducer

Dextromethorphan HBr 20 mg

Triprolidine HCl 2.5 mg

Cough suppressant

Antihistamine

Uses

MAXIMUM STRENGTH COLD, FLU & SORE THROAT

temporarily relieves these common cold and flu symptoms:
cough
nasal congestion
minor aches and pains
sore throat
headache
stuffy nose
sinus congestion and pressure
temporarily reduces fever
temporarily promotes nasal and for sinus drainage
helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive

Warnings

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

more than6 doses in 24 hours which is the maximum daily amount
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 warnings: 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.

If pregnant or breast-feeding, ask a health professional before use.

Keep out of reach of children

Overdose warnings.

Taking more than the recommended dose (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. Quick medical attention is critical for adults as well as for children even if you don’t notice any signs or symptoms.

Directions

do not take more than directed (see Overdose warning)
do not take more than 6 doses in any 24- hour period
measure only with dosing cup provided
do not use dosing cup with other products
dose as follows or as directed by a doctor
mL = milliliter
adults and children 12 years of age and over: 20 mL in dosing cup provided every 4 hours
children under 12 years of age: Do not use

Other information

each 20 mL contains: sodium 8 mg
store at room temperature
do not refrigerate

Inactive ingredients (Maximum strength Cold, Flu and Sore Throat)

anhydrous citric acid, edetate disodium, FD&C Blue No.1, FD&C Red No. 40, flavors, potassium citrate, propylene glycol, propyl gallate, purified water, sodium benzoate, sorbitol, sucralose, xanthan gum

Uses (OVERNIGHT COLD & FLU

temporarily relieves these common cold and flu symptoms:
cough
minor aches and pains
sore throat
headache
runny nose
sneezing
itching of the nose or throat
itchy, watery eyes due to hay fever
temporarily reduces fever
controls cough to help you get to sleep

Warnings

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

more than 4000 mg in 24 hours, which is the maximum daily amount
with other drugs containing acetaminophen
3 or more alcoholic drinks daily while using this product

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 (overdose) may cause liver damage. In case of overdose, get medical help or contact a Poison Control Centre right away at 1-800-222-1222.

Quick medical attention is critical for adults as well as for children, even if you do not notice any signs

Directions

do not take more than directed (see overdose warnings
do not take more than 4 doses in any 24-hour period
measure only with dosing cup provided
do not use dosing cup with other products
dose as follows or as directed by a doctor
adults and children 12 years of age and over: 20 ml in dosing cup provided every 4 hours
children under 12 years of age: do not use

Other Information

each 20 mL contains: sodium 10 mg
low sodium
store at room temperature
do not refrigerate

Inactive ingredients (Overnight Cold & Flu)

anhydrous citric acid, ascorbic acid, edetate disodium, FD&C Blue No. 1, FD&C Red No. 40, flavors, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose and xanthan gum

Questions or comments?

(1-866-467-2748)

PRINCIPAL DISPLAY PANEL - Kit Carton

VALUE PACK

NDC 11673-691-12

Compare to active ingredients Maximum Strength Mucinex® Fast Max® Cold, Flu and Sore Throat

Maximum Strength

Cold, Flu and Sore Throat

Acetaminophen • Pain Reliever/Fever Reducer

Dextromethorphan HBr • Cough Suppressant
Guaifenesin • Expectorant

Phenylephrine HCl • Nasal Decongestant

Controls Cough, Thins & Loosens Mucus
Nasal & Chest Congestion
Sinus pressure & Congestion
Body Pain, Headache, Fever & Sore Throat

*Per 4-hour dose

For Ages 12+

6 FL. OZ. (180 mL)

*This product is not manufactured or distributed by Reckitt Benckiser, the distributor of Maximum Strength Mucinex® Fast-Max® Cold, Flu & Sore Throat.

Compare to Mucinex® Nightshift Cold, Flu & Sore Throat Active Ingredients**

Overnight Cold & Flu

Acetaminophen • Pain Reliever/Fever Reducer
Dextromethorphan HBr • Cough Suppressant

Triprolidine HCl • Antihistamine

Night Time Relief for a Better Morning

Maximum Strength per 4-hour dose

Cough
Fever
Sore Throat
Runny Nose
Sneezing

For Ages 12+

6 FL OZ (180 mL)

**This product is not manufactured or distributed by RB Health, the distributor of Mucinex® Nightshift Cold & Flu.

TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING.

See bottle for full labeling

Distributed by:

094 14 8715 R00

C-001227-01-055

Dist. By Target Corp.

Mpls., MN 55403

TM & © 2020

Target Brands, Inc.

Questions?

Cal 1-866-467-2748

DO NOT TAKE MAXIMUM STRENGTH COLD, FLU & SORE THROAT & OVERNIGHT COLD & FLU LIQUIDS AT THE SAME TIME.

Target Max Strength Value Pack Cold and Flu Relief
TARGET MAXIMUM STRENGTH COLD FLU AND SORE THROAT  OVERNIGHT COLD AND FLU
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and triprolidine hcl kit
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-691
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11673-691-121 in 1 CARTON; Type 0: Not a Combination Product03/30/2020
Quantity of Parts
Part #Package QuantityTotal Product Quantity
Part 11 BOTTLE 180 mL
Part 21 BOTTLE 180 mL
Part 1 of 2
MAXIMUM STRENGTH COLD FLU AND SORE THROAT 
acetaminophen, dextromethorphan hbr, guaifenesin and phenylephrine hcl solution
Product Information
Item Code (Source)NDC:82442-737
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg  in 20 mL
Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide20 mg  in 20 mL
Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ) Guaifenesin400 mg  in 20 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE10 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
FD&C Blue No. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
POTASSIUM CITRATE (UNII: EE90ONI6FF)  
propylene glycol (UNII: 6DC9Q167V3)  
propyl gallate (UNII: 8D4SNN7V92)  
water (UNII: 059QF0KO0R)  
sodium benzoate (UNII: OJ245FE5EU)  
sorbitol (UNII: 506T60A25R)  
sucralose (UNII: 96K6UQ3ZD4)  
xanthan gum (UNII: TTV12P4NEE)  
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorFRUITImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-737-06180 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/30/2020
Part 2 of 2
TARGET OVERNIGHT COLD AND FLU 
acetaminophen, dextromethorphan hbr, phenylephrine hcl and triprolidine hcl solution
Product Information
Item Code (Source)NDC:82442-698
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen650 mg  in 20 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE20 mg  in 20 mL
TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE2.5 mg  in 20 mL
Inactive Ingredients
Ingredient NameStrength
anhydrous citric acid (UNII: XF417D3PSL)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
edetate disodium (UNII: 7FLD91C86K)  
FD&C Blue No. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
glycerin (UNII: PDC6A3C0OX)  
propyl gallate (UNII: 8D4SNN7V92)  
propylene glycol (UNII: 6DC9Q167V3)  
water (UNII: 059QF0KO0R)  
sodium benzoate (UNII: OJ245FE5EU)  
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)  
sorbitol (UNII: 506T60A25R)  
sucralose (UNII: 96K6UQ3ZD4)  
xanthan gum (UNII: TTV12P4NEE)  
Product Characteristics
ColorBLUEScore    
ShapeSize
FlavorFRUITImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:82442-698-06180 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/30/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01203/30/2020
Labeler - TARGET CORPORATION (006961700)

Revised: 4/2024
Document Id: 54683901-bfbe-4a5a-bc34-1e69eb219d13
Set id: 6e94fdab-27ea-4c0f-a91c-735ce697304b
Version: 5
Effective Time: 20240417
 
TARGET CORPORATION