COLD AND FLU NIGHT-TIME MULTI SYMPTOM RELIEF CHERRY- acetaminophen, dextromethorphan hbr, doxylamine succinate liquid 
Pharmacy Value Alliance, LLC

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Cold & Flu Night-time Multi Symptom Relief

Drug Facts

Active ingredients  (in each 30 mL dose cup)
Acetaminophen             650 mg
Dextromethorphan HBr   30 mg
Doxylamine Succinate     12.5 mg

Purpose
Acetaminophen              Pain reliever/fever reducer
Dextromethorphan HBr  Cough suppressant
Doxylamine Succinate    Antihistamine

Uses temporarily relieves cold/flu symptoms: • sore throat
• headache • minor aches and pain • fever • runny nose and
sneezing • 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, which is the maximum daily amount
• 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
two 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. • to make a child sleepy

Ask a doctor before use if you have • a sodium restricted diet
• liver disease • glaucoma • cough that occurs with too much
phlegm (mucus) • a breathing problem or chronic cough that lasts or as occurs with
smoking, asthma, chronic bronchitis or emphysema
• trouble urinating due to enlarged prostate gland.

Ask a doctor or pharmacist before use • if you are taking sedatives
or tranquilizers • if you are taking the blood thinning drug warfarin

When using this product do not use more than directed
• avoid alcoholic drinks • excitability may occur, especially in children
• marked drowsiness may occur
• be careful when driving a motor vehicle or operating machinery
• alcohol, sedatives, and tranquilizers may increase drowsiness

Stop use and ask a doctor if • redness or swelling is present
• symptoms do not get better within 7 days or are accompanied by a fever
• fever gets worse or lasts more than 3 days • new symptoms occur
• cough lasts more than 7 days, comes back, or occurs with fever, 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.

Keep out of reach of children.

Overdose warning: Taking more than the recommended dose can
cause serious health problems. 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• take only as recommended-see Overdose
warning • Use dose cup or tablespoon ([BSP) • do not exceed
4 doses per 24 hours • If taking Night Time at night and Day
Time during the day, limit total to 4 doses per 24 hours.

adults & children 12           30 mL (2 TBSP)
years and over                       every 6 hours

children 4 to                           ask a doctor
under 12 years

children under 4 years            do not use

Other information • each 30 mL dose cup
contains: sodium 45 mg • store at room temperature

Inactive ingredientscitric acid, FD&C Blue No.1,
FD&C Red No. 40, flavor, glycerin, polyethylene glycol,
propylene glycol, purified water, saccharin sodium sodium
benzoate, sodium citrate, sucrose

Questions? Call weekdays from 9:30 am to 4:30 pm EST.
1·877-798-5944.

Principal Display Panel

Premier Value®

COMPARE TO THE ACTIVE
INGREDIENTS IN
VICKS® NYQUIL®*

COLD & FLU
Night-time Multi-Symptom Relief

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

Cherry Flavor

8 FL OZ (237 mL)

INDEPENDENTLY TESTED
PV
SATISFACTION GUARANTEED

Questions? Call weekdays 1-877-798-5944.
*This product is not manufactured or distributed by Proctor &
Gamble, owner of the registered trademark Vicks® NyQuil®.

DISTRIBUTED BY: PHARMACY VALUE ALLIANCE, LLC
407 EAST LANCASTER AVENUE, WAYNE PA 19087
If for any reason you are not satisfied with this product, please
return It to the store where purchased for a full refund.

LR-025  REV 01

Product Label - Cold & Flu Night-time Multi Symptom Relief Cherry - 8 OZ Package

image description

Product Label - Cold & Flu Night-time Multi Symptom Relief Cherry - 12 OZ Package

image description

                                             Premier Value® Cold & Flu Night-time Multi Symptom Relief Cherry

COLD AND FLU NIGHT-TIME MULTI SYMPTOM RELIEF  CHERRY
acetaminophen, dextromethorphan hbr, doxylamine succinate liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68016-237
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN650 mg  in 30 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE30 mg  in 30 mL
DOXYLAMINE SUCCINATE (UNII: V9BI9B5YI2) (DOXYLAMINE - UNII:95QB77JKPL) DOXYLAMINE SUCCINATE12.5 mg  in 30 mL
Inactive Ingredients
Ingredient NameStrength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
GLYCERIN (UNII: PDC6A3C0OX)  
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)  
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
WATER (UNII: 059QF0KO0R)  
SACCHARIN SODIUM (UNII: SB8ZUX40TY)  
SODIUM BENZOATE (UNII: OJ245FE5EU)  
SODIUM CITRATE (UNII: 1Q73Q2JULR)  
SUCROSE (UNII: C151H8M554)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:68016-237-08237 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2018
2NDC:68016-237-12354 mL in 1 BOTTLE; Type 0: Not a Combination Product10/01/2018
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01210/01/2018
Labeler - Pharmacy Value Alliance, LLC (101668460)
Registrant - AptaPharma Inc. (790523323)
Establishment
NameAddressID/FEIBusiness Operations
AptaPharma Inc.790523323manufacture(68016-237)

Revised: 12/2023
Document Id: b29fb6b7-ff03-41cf-9bb2-a36060bda3f7
Set id: ada050c3-b746-4172-afcc-b48d29d52c70
Version: 4
Effective Time: 20231229
 
Pharmacy Value Alliance, LLC