WALGREEN DAYTIMEL KIDS COLD COUGH PLUS MUCUS- guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide liquid

Walgreen Daytimel Kids by

Drug Labeling and Warnings

Walgreen Daytimel Kids by is a Otc medication manufactured, distributed, or labeled by WALGREENS CO.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients (in each 15 mL)

Dextromethorphan HBr 10 mg
Guaifenesin 100 mg

Phenylephrine HCl 5 mg

Purpose

Cough suppressant
Expectorant

Nasal decongestant

Uses

• ▪ temporarily relieves common cold symptoms:
• ▪ nasal congestion
• ▪ sinus congestion & pressure
• ▪ cough due to minor throat & bronchial irritation
• ▪ cough to help you sleep
• ▪ reduces swelling of nasal passages
• ▪ temporarily restores freer breathing through the nose
• ▪ promotes nasal and/or sinus drainage
• ▪ helps loosen phlegm (mucus) and thin bronchial secretions to rid the bronchial passageways of bothersome mucus and make coughs more productive..

Warnings

Do not use

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

• ▪ heart disease
• ▪ high blood pressure
• ▪ thyroid disease
• ▪ diabetes
• ▪ trouble urinating due to 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

When using this product, do not use more than directed.

Stop use and ask a doctor if

• ▪ you get nervous, dizzy or sleepless
• ▪ symptoms do not improve within 7 days or occur with a fever
• ▪ cough persists for more than 7 days, comes back or occurs with a fever, rash or persistent headache

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 at 1-800-222-1222.

Directions

• ▪ take only as directed
• ▪ use dose cup provided
• ▪ do not exceed 4 doses per 24 hrs

adults & children 12 yrs & over 30 mL every 4 hrs

children 6 to under 12 yrs 15 mL every 4 hrs

children 4 to under 6 yrs ask a doctor

children under 4 yrs do not use

Other information

• ▪ each 15 mL contains: sodium 12 mg
• ▪ store at room temperature

Inactive ingredients

citric acid, carboxymethyl cellulose sodium, D&C Yellow No. 10, disodium edetate, FD&C Green No. 3, FD&C Red No. 40, FD&C Yellow No. 6, flavor, glycerin, propyl gallate, propylene glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

Questions?

1-866-467-2748

SPL UNCLASSIFIED SECTION

Distributed by:

PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label

Compare to the active ingredients in Kids Vicks ® DayQuil™ Honey Cold & Cough + Mucus

NDC: 0363-6238-08

Daytime

Kid’s

Cold & Cough + Mucus

Guaifenesin, Phenylephrine HCl, Dextromethorphan HBr

• Chest Congestion
• Nasal Congestion
• Cough

No Added Alcohol & Acetaminophen free

Honey Flavor

Naturally and Artificially Flavored

8 FL OZ (236 mL)

*This product is not manufactured or distributed by Procter & Gamble, the distributor of Kids Vicks ® DayQuil™ Honey Cold & Cough + Mucus.

INGREDIENTS AND APPEARANCE

WALGREEN DAYTIMEL KIDS  COLD COUGH PLUS MUCUS
guaifenesin, phenylephrine hydrochloride and dextromethorphan hydrobromide liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 0363-6238
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS)	DEXTROMETHORPHAN HYDROBROMIDE	10 mg  in 15 mL
GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ)	GUAIFENESIN	100 mg  in 15 mL
PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV)	PHENYLEPHRINE HYDROCHLORIDE	5 mg  in 15 mL

Inactive Ingredients
Ingredient Name	Strength
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
D&C YELLOW NO. 10 (UNII: 35SW5USQ3G)
EDETATE DISODIUM (UNII: 7FLD91C86K)
FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
FD&C RED NO. 40 (UNII: WZB9127XOA)
FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYL GALLATE (UNII: 8D4SNN7V92)
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	brown	Score
Shape		Size
Flavor	HONEY	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 0363-6238-08	236 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	03/01/2023

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	03/01/2023

Labeler - WALGREENS CO. (008965063)