Label: WALGREENS DAY AND NIGHT PACK- dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kit
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Contains inactivated NDC Code(s)
NDC Code(s): 0363-7570-08 - Packager: WALGREEN CO
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: OTC monograph final
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.
Drug Label Information
Updated January 12, 2022
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Children’s Daytime Wal-Tussin® DM
- Active ingredients Day Time (in each 20 mL)
- Children’s Nighttime Wal-Tussin® DM
- Active ingredients for Nighttime (in each 10 mL)
- Purposes for Daytime Wal-Tussin® DM
- Purpose for Nighttime Wal-Tussin® DM
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Uses
DAYTIME
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- temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
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- helps loosen phlegm (mucus) and thin bronchial secretions to drain bronchial tubes
NIGHTTIME
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- temporarily relieves cough due to minor throat and bronchial irritation as may occur with a cold
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- temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
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- runny nose
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- sneezing
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- itching of the nose or throat
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- itchy, watery eyes
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Warnings
Do not us
DAYTIME
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- 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
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- to sedate a child or to make a child sleepy
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- 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
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- cough that occurs with too much phlegm (mucus)
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- cough that lasts or is chronic such as occurs with smoking, asthma, chronic bronchitis or emphysema
NIGHTTIME
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- trouble urinating due to an enlarges prostate gland
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- glaucoma
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- a cough that occurs with too much phlegm (mucus)
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- a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema
When using this product
NIGHTTIME
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- do not use more than directed.
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- marked drowsiness may occur
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- avoid alcoholic drinks
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- alcohol, sedatives and tranquilizers may increase drowsiness
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- be careful when driving a motor vehicle or operating machinery
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- excitability may occur, especially in children
Stop use and ask a doctor if
DAYTIME
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- 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
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- 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.
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Directions
Daytime Wal-Tussin® DM
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- do not take more than 6 doses in any 24-hour period
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- measure only with dosing cup provided.
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- keep dosing cup with product
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- 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
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- measure only with dosing cup provided.
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- keep dosing cup with product
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- 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
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Other information
DAYTIME Wal-Tussin DM
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- each 20 mL contains: sodium 11 mg
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- store at room temperature. Do not refrigerate
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- contain low sodium
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- do not use if printed seal under cap is torn or missing
Nighttime Wal-Tussin DM
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- each 10 mL contains: sodium 6 mg
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- store at room temperature. Do not refrigerate
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- contain low sodium
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- do not use if printed seal under cap is torn or missing
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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?
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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
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- 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.
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INGREDIENTS AND APPEARANCE
WALGREENS DAY AND NIGHT PACK
dextromethorphan hbr, guaifenesin, chlorpheniramine maleate kitProduct 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 liquidProduct 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 (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 liquidProduct 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)
