Label: WALGREENS- childrens stuffy nose and cold solution
- NDC Code(s): 0363-7480-04
- Packager: WALGREENS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated November 11, 2024
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- Official Label (Printer Friendly)
- Drug Facts
- Purposes
- Uses
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Warnings
Do not use in a child who is 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 child’s prescription drug contains an MAOI, ask a doctor or pharmacist before giving this product. Avoid foods or beverages that contain caffeine.
- Ask a doctor before use if the child has
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
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Directions
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- do not give more than 6 doses in any 24 hour period
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- measure only with dosing cup provided
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- do not use dosing cup with other products
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- mL= milliliter
Age
Dose
Children 6 years to under 12 years
10 mL every 4 hours
Children 4 years to under 6 years
5 mL every 4 hours
Children under 4 years
do not use
- Other information
- Inactive ingredients
- Questions or Comments?
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Package Label-Principal Display Panel 4 FL OZ (118 mL Bottle)
Walgreens
Compare to Children’s Mucinex® Stuffy Nose & Cold active ingredients††
NDC 0363-7480-04Children's Dye-Free Stuffy Nose & Cold
GUAIFENESIN, USP 100 mg/EXPECTORANT
PHENYLEPHRINE HCl, USP 2.5 mg/NASAL DECONGESTANT
DYE FREE
ALCOHOL FREE
- •
- Relief from stuffy nose & chest congestion
- •
- Breaks up mucus
4 YEARS & OLDER
Mixed Berry FlavorNATURALLY AND ARTIFICIALLY FLAVORED
4 FL OZ (118 mL)
DOSAGE CUP PROVIDED
TAMPER-EVIDENT: DO NOT USE IF PRINTED INNER SEAL UNDER CAP IS TORN OR MISSING
IMPORTANT: KEEP THIS CARTON FOR FUTURE REFERENCE ON FULL LABELING.
DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015
Walgreens
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Walgreens.com © 2019 Walgreen Co.
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INGREDIENTS AND APPEARANCE
WALGREENS
childrens stuffy nose and cold solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-7480 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 100 mg in 5 mL PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 2.5 mg in 5 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) 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 PINK (Pink to Red) Score Shape Size Flavor BERRY, MANGO, PINEAPPLE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-7480-04 1 in 1 CARTON 05/15/2019 1 118 mL in 1 BOTTLE; 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 05/15/2019 Labeler - WALGREENS CO. (008965063)