24-7 LIFE BY 7-ELEVEN NIGHTTIME COLD AND FLU- acetaminophen, dextromethorphan hbr, doxylamine succinate solution solution

24-7 Life BY 7-ELEVEN Nighttime Cold and Flu by

Drug Labeling and Warnings

24-7 Life BY 7-ELEVEN Nighttime Cold and Flu 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 30 mL)

Acetaminophen 650 mg

Dextromethorphan HBr 30 mg

Doxylamine succinate 12.5 mg

Purpose

​Purpose

Pain reliever/fever reducer

Cough suppressant

Antihistamine

Uses

Uses

• temporarily relieves common cold and flu symptoms:
• runny nose and sneezing
• minor aches and pains
• headache
• sore throat
• 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 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

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 you have

• difficulty in urination due to enlargement of the prostate gland
• cough that occurs with too much phlegm (mucus)
• liver disease
• glaucoma
• a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis, or emphysema

Ask a doctor or pharmacist

Ask a doctor or pharmacist before use if you are

• taking the blood thinning drug warfarin
• taking sedatives or tranquilizers

When using this product

When using this product

• excitability may occur, especially in children
• avoid alcoholic beverages
• marked drowsiness may occur
• alcohol, sedatives, and tranquilizers may increase drowsiness
• use caution when driving a motor vehicle or operating machinery

Stop use and ask a doctor

Stop use and ask a doctor if

• pain or cough gets worse or lasts more than 7 days
• 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

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 6 hours
• children under 12 years: do not use

Other information

Other information

• each 30 mL contains: sodium 22 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, D&C yellow #10, FD&C green #3, FD&C yellow #6, flavors, glycerin, high fructose corn syrup, polyethylene glycol, propylene glycol, purified water, sodium benzoate, sodium chloride, sodium citrate dihydrate, sodium saccharin, sucralose

Questions or comments?

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

Nighttime Cold & Flu, 24-7 Life BY 7-ELEVEN TM

24/7 life

BY 7-ELEVEN

Cold&Flu
Nighttime Relief

Acetaminophen / Pain Reliever/Fever Reducer
Dextromethorphan HBr / Cough Suppressant
Doxylamine Succinate / Antihistamine

Relieves: Headache, Fever, Sore
Throat, Minor Aches & Pains,
Sneezing, Runny Nose, Cough

Ages 12 Years
and Over

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

12 FL OZ
(355 mL)

Eucalyptus
Mint Flavor

[image of eucalyptus leaves]

INGREDIENTS AND APPEARANCE

24-7 LIFE BY 7-ELEVEN NIGHTTIME COLD AND FLU 
acetaminophen, dextromethorphan hbr, doxylamine succinate solution solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 66715-6416
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	30 mg  in 30 mL
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	650 mg  in 30 mL
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL)	DOXYLAMINE SUCCINATE	12.5 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
SUCRALOSE (UNII: 96K6UQ3ZD4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
SODIUM SACCHARIN (UNII: SB8ZUX40TY)
TRISODIUM CITRATE DIHYDRATE (UNII: B22547B95K)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
WATER (UNII: 059QF0KO0R)
GLYCERIN (UNII: PDC6A3C0OX)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
SODIUM CHLORIDE (UNII: 451W47IQ8X)
HIGH FRUCTOSE CORN SYRUP (UNII: XY6UN3QB6S)
SODIUM BENZOATE (UNII: OJ245FE5EU)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)

Product Characteristics
Color	green	Score
Shape		Size
Flavor	MINT ((Eucalyptus mint))	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 66715-6416-4	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)