Label: WALGREENS COLD COUGH AND FLU RELIEF- acetaminophen, dextromethorphan hydrobromide liquid
- NDC Code(s): 0363-8100-12
- Packager: WALGREENS CO.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 1, 2025
If you are a consumer or patient please visit this version.
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- Official Label (Printer Friendly)
- Active Ingredients (in each 30 mL)
- Purpose
- INDICATIONS & USAGE
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WARNINGS
Warnings
Liver warning:This product contains acetaminophen. Severe liver damage may occur if you take
• 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
Allergy alert:Acetaminophen may cause severe skin or severe allergic reactions. Symptoms may include:- skin reddening
- blisters
- rash
- hives
- facial swelling
- asthma (wheezing)
- shock
If a skin or general allergic 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
- 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 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.
- if you have ever had an allergic reaction to this product or any of its ingredients
- in children under 12 years of age
Ask a doctor before use if you have
- liver disease
- persistent or chronic cough such as occurs with smoking, asthma or emphysema
- cough that is accompanied with excessive phlegm (mucus)
- a sodium-restricted diet
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
- INACTIVE INGREDIENT
- QUESTIONS
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PRINCIPAL DISPLAY PANEL
Walgreens
Compare to the active ingredients in Coricidin® HBP Maximum Strength††
NDC# 0363-8100-12
Cold, Cough & Flu Relief
ACETAMINOPHEN 650 mg /PAIN RELIEVER/FEVER REDUCER
DEXTROMETHORPHAN HBr 20 mg /COUGH SUPPRESSANT
Maximum Strength
- For relief of sore throat, fever, headache, cough, body aches & pains
- Cold relief for people with high blood pressure*
- sugar free
- Alcohol Free
Natural Cherry flavor
*Decongestant free
Maximum Strength per 4-hour dose
12 FL OZ (355 mL)
†Our pharmacist recommend the Walgreens brand. We invite you to compare to national brands.
††This product is not manufactured or distributed by Bayer Healthcare LLC, owner of the registered trademark Coricidin® HBP.
DISTRIBUTED BT: WALGREEN CO.,
DEERFIELD, IL 60015
100% SATISFACTION GUARANTEED
Walgreens.com
©2025 Walgreen Co.
MADE IN THE U.S.A. WITH DOMESTIC AND IMPORTED INGREDIENTS
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INGREDIENTS AND APPEARANCE
WALGREENS COLD COUGH AND FLU RELIEF
acetaminophen, dextromethorphan hydrobromide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-8100 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 650 mg in 30 mL DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 20 mg in 30 mL Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) EDETATE DISODIUM (UNII: 7FLD91C86K) FD&C BLUE NO. 1 (UNII: H3R47K3TBD) FD&C RED NO. 40 (UNII: WZB9127XOA) GLYCERIN (UNII: PDC6A3C0OX) POLOXAMER 105 (UNII: XPP85ZHV76) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) POTASSIUM CITRATE (UNII: EE90ONI6FF) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) XANTHAN GUM (UNII: TTV12P4NEE) Product Characteristics Color red Score Shape Size Flavor CHERRY Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-8100-12 355 mL in 1 BOTTLE; Type 0: Not a Combination Product 04/01/2025 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 04/01/2025 Labeler - WALGREENS CO. (008965063)
