Label: VICKS DAYQUIL SEVERE COLD AND FLU- Acetaminophen ...

Label: VICKS DAYQUIL SEVERE COLD AND FLU- acetaminophen, phenylephine hcl, dextromethorphan hydrobromide, and guaifenesin capsule, liquid filled

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• NDC Code(s): 37000-517-02, 37000-517-08, 37000-517-16, 37000-517-24
• Packager: The Procter & Gamble Manufacturing Company

• Category: HUMAN OTC DRUG LABEL
• DEA Schedule: None

Drug Label Information

Updated February 5, 2026

If you are a consumer or patient please visit this version.

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• SPL UNCLASSIFIED SECTION

  Drug Facts

• Active ingredients (in each LiquiCap)

  Acetaminophen 325 mg

  Dextromethorphan HBr 10 mg

  Guaifenesin 200 mg

  Phenylephrine HCl 5 mg

  Purpose

  Pain reliever/fever reducer

  Cough suppressant

  Expectorant

  Nasal decongestant

• Uses
  • temporarily relieves common cold/flu symptoms:
  • nasal congestion
  • sinus congestion & pressure
  • cough due to minor throat & bronchial irritation
  • minor aches & pains
  • headache
  • fever
  • sore throat
  • 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

  Liver warning:

  This product contains acetaminophen. Severe liver damage may occur if you take

  • more than 8 LiquiCaps in 24 hours, which is the maximum daily amount for this product
  • with other drugs containing acetaminophen
  • 3 or more alcoholic drinks daily while using this product

  Allergy Alert:

  Acetaminophen may cause severe skin reactions. Symptoms may include:

  • Skin reddening
  • Blisters
  • Rash

  If a skin 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.

  Ask a doctor before use if you have

  • liver disease
  • 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

  Ask a doctor or pharmacist before use if you are

  taking the blood thinning drug warfarin

  When using this product, do not use more than directed

  Stop use and ask a doctor if

  • you get nervous, dizzy or sleepless
  • pain, nasal congestion, or cough gets worse or lasts more than 7 days
  • fever gets worse or lasts more than 3 days
  • redness or swelling is present
  • new symptoms occur
  • cough comes back or occurs with rash or headache that lasts.

  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.

  In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms.

• Directions
  • take only as directed
  • do not exceed 8 LiquiCaps per 24 hrs

  adults & children 12 yrs & over	2 LiquiCaps with water every 4 hrs
  children 4 to under 12 yrs	ask a doctor
  children under 4 yrs	do not use

• Other information
  • store at no greater than 25ºC
• Inactive ingredients

  ascorbic acid, FD&C Blue No. 1, FD&C Red No. 40, gelatin, glycerin, mannitol, polyethylene glycol, povidone, propylene glycol, shellac, simethicone, sorbitan, sorbitol, titanium dioxide, water

• Questions?

  1-800-362-1683

• SPL UNCLASSIFIED SECTION

  TAMPER EVIDENT: This package is safety-sealed & child resistant. Use only if blisters are intact. If difficult to open, use scissors.

• SPL UNCLASSIFIED SECTION

  Made in Canada

  DIST. BY PROCTER & GAMBLE, CINCINNATI OH 45202

• PRINCIPAL DISPLAY PANEL - 24 LiquiCapd Carton

  MAX

  STRENGTH

  VICKS®

  DayQuil™

  SEVERE

  COLD & FLU

  Acetaminophen, Guaifenesin, Phenylephrine HCl, Dextromethorphan HBr

  Headache, Fever, Sore Throat, Minor Aches & Pains Chest Congestion, Thins & Loosens Mucus Nasal Congestion, Sinus Pressure Cough

  Non-Drowsy

  24 LIQUICAPS™

  

• INGREDIENTS AND APPEARANCE

  VICKS DAYQUIL SEVERE  COLD AND FLU acetaminophen, phenylephine hcl, dextromethorphan hydrobromide, and guaifenesin capsule, liquid filled

  Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:37000-517 Route of Administration ORAL

  Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PHENYLEPHRINE HYDROCHLORIDE (UNII: 04JA59TNSJ) (PHENYLEPHRINE - UNII:1WS297W6MV) PHENYLEPHRINE HYDROCHLORIDE 5 mg ACETAMINOPHEN (UNII: 362O9ITL9D) (ACETAMINOPHEN - UNII:362O9ITL9D) ACETAMINOPHEN 325 mg DEXTROMETHORPHAN HYDROBROMIDE (UNII: 9D2RTI9KYH) (DEXTROMETHORPHAN - UNII:7355X3ROTS) DEXTROMETHORPHAN HYDROBROMIDE 10 mg GUAIFENESIN (UNII: 495W7451VQ) (GUAIFENESIN - UNII:495W7451VQ) GUAIFENESIN 200 mg

  Inactive Ingredients Ingredient Name Strength MANNITOL (UNII: 3OWL53L36A)   SORBITAN (UNII: 6O92ICV9RU)   GLYCERIN (UNII: PDC6A3C0OX)   ASCORBIC ACID (UNII: PQ6CK8PD0R)   SHELLAC (UNII: 46N107B71O)   FD&C RED NO. 40 (UNII: WZB9127XOA)   FD&C BLUE NO. 1 (UNII: H3R47K3TBD)   GELATIN (UNII: 2G86QN327L)   POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)   POVIDONE (UNII: FZ989GH94E)   PROPYLENE GLYCOL (UNII: 6DC9Q167V3)   WATER (UNII: 059QF0KO0R)   TITANIUM DIOXIDE (UNII: 15FIX9V2JP)   DIMETHICONE (UNII: 92RU3N3Y1O)   SORBITOL (UNII: 506T60A25R)

  Product Characteristics Color orange Score no score Shape BULLET Size 16mm Flavor Imprint Code DS Contains

  Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:37000-517-24 2 in 1 CARTON 07/10/2018 1 12 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:37000-517-16 2 in 1 CARTON 07/10/2018 2 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:37000-517-08 1 in 1 CARTON 07/01/2019 3 8 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:37000-517-02 2 in 1 POUCH; Type 0: Not a Combination Product 01/01/2021

  Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M012 07/10/2018

  Labeler - The Procter & Gamble Manufacturing Company (004238200)

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More Info on this Drug

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VICKS DAYQUIL SEVERE COLD AND FLU- acetaminophen, phenylephine hcl, dextromethorphan hydrobromide, and guaifenesin capsule, liquid filled

Number of versions: 18

Published Date (What is this?)	Version	Files
Feb 6, 2026	18 (current)	download
Oct 3, 2025	17	download
Aug 8, 2025	16	download
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Jul 10, 2018	1	download

VICKS DAYQUIL SEVERE COLD AND FLU- acetaminophen, phenylephine hcl, dextromethorphan hydrobromide, and guaifenesin capsule, liquid filled

Under Review - Editing is pending for RxNorm. If in scope, these drugs will include RxNorm normal forms when editing is complete.

VICKS DAYQUIL SEVERE COLD AND FLU- acetaminophen, phenylephine hcl, dextromethorphan hydrobromide, and guaifenesin capsule, liquid filled

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VICKS DAYQUIL SEVERE COLD AND FLU- acetaminophen, phenylephine hcl, dextromethorphan hydrobromide, and guaifenesin capsule, liquid filled

If this SPL contains inactivated NDCs listed by the FDA initiated compliance action, they will be specified as such.

NDC
1	37000-517-02
2	37000-517-08
3	37000-517-16
4	37000-517-24

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