WAL TUSSIN CF MAX MULTI SYMPTOM COUGH COLD AND FLU acetaminophen dextromethorphan hbr guaifenesin phenylephrine hcl solution

United States - English - NLM (National Library of Medicine)

Buy It Now

Active ingredient:
ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D)
Available from:
Walgreen Company
INN (International Name):
ACETAMINOPHEN
Composition:
ACETAMINOPHEN 650 mg in 20 mL
Prescription type:
OTC DRUG
Authorization status:
OTC monograph final

WAL TUSSIN CF MAX MULTI SYMPTOM COUGH COLD AND FLU- acetaminophen,

dextromethorphan hbr, guaifenesin, phenylephrine hcl solution

Walgreen Company

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they

comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

----------

Walgreen Co. Wal-Tussin CF Max Drug Facts

Active ingredients (in each 20 mL)

Acetaminophen, USP 650 mg

Dextromethorphan HBr, USP 20 mg

Guaifenesin, USP 400 mg

Phenylephrine HCl, USP 10 mg

Purpos es

Pain reliever/fever reducer

Cough suppressant

Expectorant

Nasal decongestant

Us es

Warnings

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

Allergy alert: Acetaminophen may cause severe skin reactions. Symptoms may include:

temporarily relieves these symptoms occurring with a cold or flu:

cough due to minor throat and bronchial irritation

nasal congestion

sinus congestion and pressure

minor aches and pains

sore throat

headache

temporarily reduces fever

helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes and make

coughs more productive

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

skin reddening

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

Ask a doctor before use if you have

Ask a doctor or pharmacist before use if you are

When using this product

do not use more than directed

Stop use and ask a doctor if

blisters

rash

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.

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

liver disease

heart disease

high blood pressure

thyroid disease

diabetes

trouble urinating due to an enlarged prostate gland

cough that occurs with too much phlegm (mucus)

persistent or chronic cough such as occurs with smoking, asthma, chronic bronchitis, or

emphysema

taking the blood thinning drug warfarin

you get nervous, dizzy or sleepless

pain, cough, or nasal congestion 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.

Overdose warning: In case of overdose, get medical help or contact a Poison Control Center right away

(1-800-222-1222). Prompt medical attention is critical for adults as well as for children even if you do

not notice any signs or symptoms.

Directions

dose

adults and children

12 years and over

20 mL every 4 hours

children under 12 years

do not use

Other information

Inactive ingredients

anhydrous citric acid, benzyl alcohol, edetate disodium, FD&C red #40, flavor, glycerin, polyethylene

glycol, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol solution, sucralose,

triacetin, xanthan gum

Questions or comments?

1-800-719-9260

Package/Label Principal Display Panel

SEVERE

MAXIMUM STRENGTH

ADULT – NON-DROWSY

Wal-Tussin® CF Max

CF MAX

do not take more than 5 doses in any 24-hour period

do not exceed recommended dosage. Taking more than the recommended dose (overdose) may

cause serious liver damage.

measure only with dosing cup provided

keep dosing cup with product

mL = milliliter

this adult product is not intended for use in children under 12 years of age

each 20 mL contains: sodium 15 mg

store at 20-25 C (68-77 F). Do not refrigerate.

Multi-Symptom Cough, Cold & Flu

Acetaminophen / Pain Reliever / Fever Reducer

Dextromethorphan HBr / Cough Suppressant

Guaifenesin / Expectorant

Phenylephrine HCl / Nasal Decongestant

Relieves cough, sore throat, body aches, fever, nasal congestion & chest congestion

Ages 12 & older

4 FL OZ (118 mL)

Compare to Robitussin® Maximum Strength Severe

Multi-Symptom Cough Cold + Flu active ingredients

WAL TUSSIN CF MAX MULTI SYMPTOM COUGH COLD AND FLU

acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl solution

Product Information

Product T ype

HUMAN OTC DRUG

Ite m Code (Source )

NDC:0 36 3-0 0 51

Route of Administration

ORAL

Active Ingredient/Active Moiety

Ingredient Name

Basis of Strength

Stre ng th

ACETAMINO PHEN (UNII: 36 2O9 ITL9 D) (ACETAMINOPHEN - UNII:36 2O9 ITL9 D)

ACETAMINOPHEN

6 50 mg

in 20 mL

DEXTRO METHO RPHAN HYDRO BRO MIDE (UNII: 9 D2RTI9 KYH)

(DEXTROMETHORPHAN - UNII:7355X3ROTS)

DEXTROMETHORPHAN

HYDROBROMIDE

20 mg

in 20 mL

GUAIFENESIN (UNII: 49 5W7451VQ) (GUAIFENESIN - UNII:49 5W7451VQ)

GUAIFENESIN

40 0 mg

in 20 mL

PHENYLEPHRINE HYDRO CHLO RIDE (UNII: 0 4JA59 TNSJ) (PHENYLEPHRINE -

UNII:1WS29 7W6 MV)

PHENYLEPHRINE

HYDROCHLORIDE

10 mg

in 20 mL

Inactive Ingredients

Ingredient Name

Stre ng th

ANHYDRO US CITRIC ACID (UNII: XF417D3PSL)

BENZYL ALCO HO L (UNII: LKG8 49 4WBH)

EDETATE DISO DIUM (UNII: 7FLD9 1C8 6 K)

FD&C RED NO . 4 0 (UNII: WZB9 127XOA)

GLYCERIN (UNII: PDC6 A3C0 OX)

PO LYETHYLENE GLYCO LS (UNII: 3WJQ0 SDW1A)

PRO PYLENE GLYCO L (UNII: 6 DC9 Q16 7V3)

WATER (UNII: 0 59 QF0 KO0 R)

SO DIUM BENZO ATE (UNII: OJ245FE5EU)

SO DIUM CITRATE, UNSPECIFIED FO RM (UNII: 1Q73Q2JULR)

SUCRALO SE (UNII: 9 6 K6 UQ3ZD4)

TRIACETIN (UNII: XHX3C3X6 73)

XANTHAN GUM (UNII: TTV12P4NEE)

SO RBITO L (UNII: 50 6 T6 0 A25R)

Product Characteristics

Color

S core

S hap e

S iz e

Flavor

BERRY

Imprint Code

Contains

Packag ing

#

Item Code

Package Description

Marketing Start Date

Marketing End Date

1

NDC:0 36 3-0 0 51-26

1 in 1 CARTON

0 7/0 6 /20 16

1

118 mL in 1 BOTTLE; Type 0 : No t a Co mbinatio n Pro duct

Marketing Information

Marke ting Cate gory

Application Numbe r or Monograph Citation

Marke ting Start Date

Marke ting End Date

OTC mo no graph final

pa rt341

0 7/0 6 /20 16

Labeler -

Walgreen Company (008965063)

Walgreen Company

Revised: 7/2016

Similar products

Search alerts related to this product

Share this information