VICKS DAYQUIL HOT REMEDY RAPID RELIEF MULTI-SYMPTOM COLD AND FLU PLUS CONGESTION- acetaminophen, dextromethorphan hbr, phenylephrine hcl powder, for solution

Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM by

Drug Labeling and Warnings

Vicks DayQuil HOT REMEDY RAPID RELIEF MULTI-SYMPTOM by is a Otc medication manufactured, distributed, or labeled by Procter & Gamble Manufactura S de RL de CV. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Vicks® DayQuil™ HOT REMEDYRAPID RELIEFMULTI-SYMPTOMCOLD & FLU + CONGESTION

Drug Facts

Active Ingredients (in each Packet) 

Acetaminophen500 mg

Dextromethorphan HBr 20 mg
Phenylephrine HCl 10 mg

Purpose

Pain reliever/Fever reducer

Cough suppressant
Nasal decongestant

Uses

temporarily relieves common cold/flu symptoms:

minor aches & pains

sore throat

fever

headache

cough due to minor throat & bronchial irritation

cough to help you sleep

nasal congestion

sinus congestion & pressure

reduces swelling of nasal passages

temporarily restores freer breathing through the nose

promotes nasal and/or sinus drainage

Warnings

Liver warning:

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

• more than 6 doses in 24 hours, which is the maximum daily amount for this product
• 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 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.

Ask a doctor before use if you have

• liver disease
• heart disease
• high blood pressure
• thyroid disease
• diabetes
• cough that occurs with too much phlegm (mucus)
• persistent or chronic cough such as occurs with smoking, asthma, or emphysema
• trouble urinating due to enlarged prostate gland

Ask a doctor or pharmacist before use if you are

taking the blood thinning drug warfarin

When using this product

do not use more than directed

Stop use and ask a doctor if

• you get nervous, dizzy or sleepless
• pain, nasal congestion, 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, ask a health professional before use.

Keep out of reach of children.

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 directed

do not exceed 6 doses per 24 hrs

Dissolve contents of one packet into 8 oz. of hot water and stir briskly; sip while hot. Consume entire drink within 10-15 minutes

If using a microwave, add contents of one packet to 8 oz. of cool water, stir briskly before and after heating. Do not overheat

• Age: Dose
• adults & children 12 yrs & over: one packet (dose) every 4 hours
• children under 12 yrs: do not use

Other information

each packet contains: potassium 10 mg

phenylketonurics: contains phenylalanine 64 mg per dose

do not exceed 25°C.

Inactive ingredients

acesulfame potassium, aspartame, carboxymethylcellulose, citric acid, D&C Yellow No. 10, FD&C Blue No. 1, FD&C Red No. 40, flavors, sucrose, tribasic calcium phosphate

Questions?

1-800-362-1683

SPL UNCLASSIFIED SECTION

Tamper Evident:Do not use if sachet is opened or torn

SPL UNCLASSIFIED SECTION

MADE IN MEXICO

DIST. BY PROCTER & GAMBLE,
CINCINNATI OH 45202

PRINCIPAL DISPLAY PANEL - 8 packet package

TRIPLE ACTION

Vicks® DayQuil™ HOT REMEDY

RAPID RELIEF

MULTI-SYMPTOM

COLD & FLU + CONGESTION

Acetaminophen, Dextromethorphan HBr, Phenylephrine HCl

Headache, Fever, Sore Throat, Minor Aches & Pains

Nasal Congestion, Sinus Pressure

Cough

Non-Drowsy

HONEY LEMON FLAVORED

8 POWDER PACKETS

INGREDIENTS AND APPEARANCE

VICKS DAYQUIL HOT REMEDY RAPID RELIEF MULTI-SYMPTOM  COLD AND FLU PLUS CONGESTION
acetaminophen, dextromethorphan hbr, phenylephrine hcl powder, for solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58933-550
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)	ACETAMINOPHEN	500 mg  in 5 g
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	10 mg  in 5 g
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg  in 5 g

Inactive Ingredients
Ingredient Name	Strength
ACESULFAME POTASSIUM (UNII: 23OV73Q5G9)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
ASPARTAME (UNII: Z0H242BBR1)
SUCROSE (UNII: C151H8M554)
FD&C RED NO. 40 (UNII: WZB9127XOA)
CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)

Product Characteristics
Color	white	Score
Shape		Size
Flavor	HONEY (Lemon)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58933-550-01	5 g in 1 PACKET; Type 0: Not a Combination Product	03/22/2023
2	NDC: 58933-550-08	8 in 1 PACKAGE	03/22/2023
2		5 g in 1 PACKET; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	03/22/2023

Labeler - Procter & Gamble Manufactura S de RL de CV (812807550)