WALGREENS DAY AND NIGHT PACK- dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kit

Walgreens DAY and NIGHT PACK by

Drug Labeling and Warnings

Walgreens DAY and NIGHT PACK by is a Otc medication manufactured, distributed, or labeled by WALGREEN CO. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Children’s Daytime Wal-Tussin® DM

Active ingredients Day Time (in each 20 mL)

Dextromethorphan HBr USP 20 mg

Guaifenesin. USP 200 mg

Children’s Nighttime Wal-Tussin® DM

Active ingredients for Nighttime (in each 10 mL)

Chlorpheniramine maleate, USP 2 mg

Dextromethorphan HBr USP 15 mg

Purposes for Daytime Wal-Tussin® DM

Cough suppressant

Expectorant

Purpose for Nighttime Wal-Tussin® DM

Antihistamine

Cough suppressant

Uses

DAYTIME

• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
• helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes

NIGHTTIME

• temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
• temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
  • ▪ runny nose
  • ▪ sneezing
  • ▪ itching of the nose or throat 
  • ▪ itchy, watery eyes

Warnings

Do not us

DAYTIME

• 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.

NIGHTTIME

• to sedate a child or to make a child sleepy
• 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

DAYTIME

• cough that occurs with too much phlegm (mucus)
• cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema

NIGHTTIME

• trouble urinating due to an enlarges prostate gland
• glaucoma
• a 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

Ask a doctor or pharmacist before use if you are

NIGHTTIME

taking sedatives or tranquilizers.

When using this product

NIGHTTIME

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

Stop use and ask a doctor if

DAYTIME

• cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

NIGHTTIME

• cough last more than 7 days, comes back or is accompanied by fever, rash, or persistent headache. These could be signs of a serious condition.

If pregnant or breast-feeding,

DAYTIME

ask a health professional before use.

NIGHTTIME

ask a health professional before use

Keep out of reach of children.

DAYTIME

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

NIGHTTIME

In case of overdose, get medical help or contact a Poison Control Center (1-800-222-1222) right away

Directions

Daytime Wal-Tussin® DM

• do not take more than 6 doses in any 24-hour period
• measure only with dosing cup provided.
• keep dosing cup with product
• mL= milliliter

• age:

  dose

• Children under 4 years:

  Do not use

• Children 4 to under 6 years:

  5 mL every 4 hours

• Children 6 to under 12 years:

  10 mL every 4 hours

• Adults and children 12 years and older:

  20 mL every 4 hours

Nighttime Wal-Tussin® DM

• do not take more than 4 doses in any 24-hour period
• measure only with dosing cup provided.
• keep dosing cup with product
• mL= milliliter

• age:

  dose

• Children under 6 years:

  Do not use

• Children 6 to under 12 years:

  10 mL every 6 hours

• Adults and children 12 years and older:

  20 mL every 6 hours

Other information

DAYTIME Wal-Tussin DM

• each 20 mL contains: sodium 11 mg
• store at room temperature. Do not refrigerate
• contain low sodium
• do not use if printed seal under cap is torn or missing

Nighttime Wal-Tussin DM

• each 10 mL contains: sodium 6 mg
• store at room temperature. Do not refrigerate
• contain low sodium
• do not use if printed seal under cap is torn or missing

Inactive ingredients

Inactive ingredients for Day Time Wal-Tussin DM 

anhydrous citric acid, carboxymethylcellulose sodium, edetate disodium, FD &C Blue No. 1, FD&C Red No. 40, natural and artificial flavors, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

Inactive ingredients for Night Time Wal-Tussin DM 

anhydrous citric acid, FD&C Red No. 40, natural and artificial flavors, glycerin, lactic acid, potassium sorbate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose

Questions or comments?

1-866-467-2748

Principal Display Panel

Compare to Children's Robitussin® Cough & Chest Congestion DM* & Nighttime Cough DM Long-Active active ingredients††

Children's

Cough & Chest Congestions DM

Wal-Tussin® DM

DEXTROMETHORPHAN HBr, USP 20 mg/ 20 mL

COUGH SUPPRESSANT

GUAIFENESIN, USP 200 mg

EXPECTORANT

DAYTIME

NON-DROWSY

Relieves cough, chest congestion & mucus

4 YEARS & OVER

GRAPE FLAVOR

Naturally and Artificially Flavored

Dosage cup included

2 - 4 FL OZ (118 mL) BOTTLES / TOTAL – 8 FL OZ (236 mL)

††This product is not manufactured or distributed by Pfizer, the distributor of Children’s Robitussin® Cough & Chest Congestion DM.

Children's

Nighttime Cough DM

Wal-Tussin® DM

CHLORPHENIRAMINE MALEATE, USP 2 mg / 10 mL

ANTIHISTAMINE

DEXTROMETHORPHAN HBr, USP 15 mg / 10 mL

COUGH SUPPRESSANT

NIGHTTIME

• Relieves cough & runny nose

Alcohol free

6 YEARS & OLDER

Fruit Punch Flavor

Naturally and Artificially Flavored

Dosage cup included

2 - 4 FL OZ (118 mL) BOTTLES TOTAL – 8 FL OZ (236 mL)

††This product is not manufactured or distributed by Pfizer, the distributor of Children’s Robitussin® Nighttime Cough DM Long-Acting.

Walgreens

PHARMACIST RECOMMENDED

TAMPER EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS BROKEN OR MISSING

DISTRIBUTED BY: WALGREENS CO.

200 WILMOT RD. DEERFIELD, IL 60015

Walgreens 10% SATISFACTION GUARANTEED

walgreens.com ©2020 Walgreen Co.

INGREDIENTS AND APPEARANCE

WALGREENS DAY AND NIGHT PACK 
dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kit

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-7570

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-7570-08	1 in 1 KIT; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)	04/13/2020

Quantity of Parts
Part #	Package Quantity	Total Product Quantity
Part 1	1 BOTTLE	118 mL
Part 2	1 BOTTLE	118 mL

Part 1 of 2

DAYTIME COUGH AND CHEST CONGESTION 
dextromethorphan hbr, guaifenesin liquid

Product Information
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	20 mg  in 20 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	200 mg  in 20 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)
EDETATE DISODIUM (UNII: 7FLD91C86K)
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)
XANTHAN GUM (UNII: TTV12P4NEE)

Product Characteristics
Color	PURPLE	Score
Shape		Size
Flavor	GRAPE	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	04/13/2020

Part 2 of 2

NIGHT TIME COUGH DM 
chlorpheniramine maleate, diphenhydramine hbr liquid

Product Information
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CHLORPHENIRAMINE MALEATE (UNII: V1Q0O9OJ9Z) (CHLORPHENIRAMINE - UNII:3U6IO1965U)	CHLORPHENIRAMINE MALEATE	2 mg  in 10 mL
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	15 mg  in 10 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
FD&C RED NO. 40 (UNII: WZB9127XOA)
GLYCERIN (UNII: PDC6A3C0OX)
LACTIC ACID, UNSPECIFIED FORM (UNII: 33X04XA5AT)
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SODIUM BENZOATE (UNII: OJ245FE5EU)
SODIUM CITRATE, UNSPECIFIED FORM (UNII: 1Q73Q2JULR)
SORBITOL (UNII: 506T60A25R)
SUCRALOSE (UNII: 96K6UQ3ZD4)

Product Characteristics
Color	RED	Score
Shape		Size
Flavor	FRUIT PUNCH	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1		118 mL in 1 BOTTLE; Type 9: Other Type of Part 3 Combination Product (e.g., Drug/Device/Biological Product)

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	04/13/2020

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part341	04/13/2020

Labeler - WALGREEN CO (008965063)