Label: TARGET MAXIMUM STRENGTH COLD FLU AND SORE THROAT OVERNIGHT COLD AND FLU- acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and triprolidine hcl kit
- NDC Code(s): 11673-691-12, 82442-698-06, 82442-737-06
- Packager: TARGET CORPORATION
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 17, 2024
If you are a consumer or patient please visit this version.
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- SPL UNCLASSIFIED SECTION
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ACTIVE INGREDIENT
Active ingredients (in each 20 mL)
MAXIMUM STRENGTH‡ COLD, FLU & SORE THROATPurposes 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
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Uses
MAXIMUM STRENGTH COLD, FLU & SORE THROAT
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- temporarily relieves these common cold and flu symptoms:
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- cough
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- nasal congestion
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- minor aches and pains
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- sore throat
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- headache
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- stuffy nose
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- sinus congestion and pressure
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- temporarily reduces fever
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- temporarily promotes nasal and for sinus drainage
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- helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive
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Warnings
Liver warnings: This product contains acetaminophen. Severe liver damage may occur if you take:
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- more than6 doses in 24 hours which is the maximum daily amount
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- with other drugs containing acetaminophen
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- 3 or more alcoholic drinks daily while using this product
Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:
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- skin reddening
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- blisters
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- 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.
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Do not use
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- with any other drug containing acetaminophen (prescription or nonprescription). If you are not sure whether a drug contains acetaminophen, ask a doctor or pharmacist.
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- 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.
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Directions
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- do not take more than directed (see Overdose warning)
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- do not take more than 6 doses in any 24- hour period
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- measure only with dosing cup provided
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- do not use dosing cup with other products
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- dose as follows or as directed by a doctor
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- mL = milliliter
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- adults and children 12 years of age and over: 20 mL in dosing cup provided every 4 hours
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- children under 12 years of age: Do not use
- Other information
- Inactive ingredients (Maximum strength Cold, Flu and Sore Throat)
- Uses (OVERNIGHT COLD & FLU
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Warnings
Liver warnings: This product contains acetaminophen. Severe liver damage may occur if you take:
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- more than 4000 mg in 24 hours, which is the maximum daily amount
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- with other drugs containing acetaminophen
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- 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
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- do not take more than directed (see overdose warnings
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- do not take more than 4 doses in any 24-hour period
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- measure only with dosing cup provided
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- do not use dosing cup with other products
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- dose as follows or as directed by a doctor
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- adults and children 12 years of age and over: 20 ml in dosing cup provided every 4 hours
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- children under 12 years of age: do not use
- Inactive ingredients (Overnight Cold & Flu)
- Questions or comments?
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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 • ExpectorantPhenylephrine HCl • Nasal Decongestant
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- Controls Cough, Thins & Loosens Mucus
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- Nasal & Chest Congestion
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- Sinus pressure & Congestion
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- 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 SuppressantTriprolidine HCl • Antihistamine
Night Time Relief for a Better Morning
Maximum Strength per 4-hour dose
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- Cough
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- Fever
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- Sore Throat
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- Runny Nose
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- 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.
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INGREDIENTS AND APPEARANCE
TARGET MAXIMUM STRENGTH COLD FLU AND SORE THROAT OVERNIGHT COLD AND FLU
acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl and triprolidine hcl kitProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:11673-691 Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:11673-691-12 1 in 1 CARTON; Type 0: Not a Combination Product 03/30/2020 Quantity of Parts Part # Package Quantity Total Product Quantity Part 1 1 BOTTLE 180 mL Part 2 1 BOTTLE 180 mL Part 1 of 2 MAXIMUM STRENGTH COLD FLU AND SORE THROAT
acetaminophen, dextromethorphan hbr, guaifenesin and phenylephrine hcl solutionProduct Information Item Code (Source) NDC:82442-737 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 650 mg in 20 mL Dextromethorphan Hydrobromide (UNII: 9D2RTI9KYH) (Dextromethorphan - UNII:7355X3ROTS) Dextromethorphan Hydrobromide 20 mg in 20 mL Guaifenesin (UNII: 495W7451VQ) (Guaifenesin - UNII:495W7451VQ) Guaifenesin 400 mg in 20 mL PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 10 mg in 20 mL Inactive Ingredients Ingredient Name Strength 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 Color BLUE Score Shape Size Flavor FRUIT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82442-737-06 180 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 03/30/2020 Part 2 of 2 TARGET OVERNIGHT COLD AND FLU
acetaminophen, dextromethorphan hbr, phenylephrine hcl and triprolidine hcl solutionProduct Information Item Code (Source) NDC:82442-698 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength Acetaminophen (UNII: 362O9ITL9D) (Acetaminophen - UNII:362O9ITL9D) Acetaminophen 650 mg in 20 mL DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 20 mL TRIPROLIDINE HYDROCHLORIDE (UNII: YAN7R5L890) (TRIPROLIDINE - UNII:2L8T9S52QM) TRIPROLIDINE HYDROCHLORIDE 2.5 mg in 20 mL Inactive Ingredients Ingredient Name Strength 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 Color BLUE Score Shape Size Flavor FRUIT Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:82442-698-06 180 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product) Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 03/30/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 03/30/2020 Labeler - TARGET CORPORATION (006961700)
