DAYTIME COLD AND FLU RELIEF, 24-7 LIFE BY 7-ELEVEN- acetaminophen, dextromethorphan hbr, phenylephrine hcl solution solution

Daytime Cold and Flu Relief, 24-7 Life BY 7-Eleven by

Drug Labeling and Warnings

Daytime Cold and Flu Relief, 24-7 Life BY 7-Eleven by is a Otc medication manufactured, distributed, or labeled by Lil' Drug Store Products, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug facts

Active ingredients

Active ingredients (in each 15 mL)

Acetaminophen 325 mg

Dextromethorphan HBr 10 mg

Phenylephrine HCl 5 mg

Purpose

Purpose

Pain reliever/fever reducer

Cough suppressant

Nasal decongestant

Uses

Uses

• temporarily relieves common cold and flu symptoms:
• sore throat
• nasal congestion
• minor aches and pains
• headache
• cough due to minor throat and bronchial irritation
• temporarily reduces fever

Warnings

Liver warning

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

• adult takes more than 4,000 mg of acetaminophen in 24 hours
• child takes more than 5 doses in 24 hours
• taken with other drugs containing acetaminophen
• adult has 3 or more alcoholic drinks every day while using this product

Allergy alert

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

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

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 you have ever had an allergic reaction to this product or any of its ingredients

Ask a doctor before use

Ask a doctor before use if the user has

• difficulty in urination due to enlargement of the prostate
• cough that occurs with too much phlegm (mucus)
• persistent or chronic cough such as occurs with smoking, asthma, or emphysema
• heart disease
• diabetes
• thyroid disease
• liver disease
• high blood pressure

Ask a doctor or pharmacist before use

Ask a doctor or pharmacist before use if the user is taking the blood thinning drug warfarin.

When using this product

When using this product do not exceed recommended dosage.

Stop use and ask a doctor

Stop use and ask a doctor if

• nervousness, dizziness, or sleeplessness occur
• fever gets worse or lasts more than 3 days
• redness or swelling is present
• new symptoms occur
• pain, nasal congestion, or cough gets worse or lasts more than 5 days (children) or 7 days (adults)
• cough comes back or occurs with rash or headache that lasts. These could be signs of a serious condition.

If pregnant or breast-feeding

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

Keep out of reach of children

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Prompt medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

Directions

Directions

• do not take more than directed
• mL = milliliter
• only use the dose cup provided
• do not exceed 4 doses per 24 hours

• adults and children 12 years and over: 30 mL every 4 hours
• children 6 to under 12 years: 15 mL every 4 hours
• children under 6 years: do not use

Other information

Other information

• each 15 mL contains: sodium 13 mg
• store at 25°C (77°F); excursions permitted between 15°-30°C (59°-86°F)
• use by expiration date on package

Inactive ingredients

Inactive ingredients

anhydrous citric acid, FD&C yellow #6, flavors, glycerin, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium citrate dihydrate, sodium etabisulfite, sodium saccharin, sorbitol, sucralose

Questions or comments?

Questions or comments? 1-877-507-6516 (8 AM – 4:30PM CST)

PRINCIPAL DISPLAY PANEL

24/7 Life

BY 7-ELEVEN TM

Cold & Flu

DayTime Relief

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

Relieves: Headache, Fever, Sore
Throat, Minor Aches & Pains,
Nasal Congestion, Cough

Ages 6 Years
and Over

compare to Vicks ®
DayQuil ® Cold & Flu
active ingredients*

12 FL OZ

(355 mL)

Menthol

Flavor

[imsge of mentha avensis leaf]

INGREDIENTS AND APPEARANCE

DAYTIME COLD AND FLU RELIEF, 24-7 LIFE BY 7-ELEVEN 
acetaminophen, dextromethorphan hbr, phenylephrine hcl solution solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66715-6415
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg  in 15 mL
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	325 mg  in 15 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
SORBITOL (UNII: 506T60A25R)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM BENZOATE (UNII: OJ245FE5EU)
WATER (UNII: 059QF0KO0R)
SODIUM METABISULFITE (UNII: 4VON5FNS3C)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
GLYCERIN (UNII: PDC6A3C0OX)
SUCRALOSE (UNII: 96K6UQ3ZD4)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)

Product Characteristics
Color	orange	Score
Shape		Size
Flavor	MENTHOL	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66715-6415-4	355 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	04/19/2022

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	04/19/2022

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