Indications and uses
temporarily relieves common cold/flu symptoms: cough due to minor throat and bronchial irritation sore throat headache minor aches and pains fever runny nose and sneezing
VICKS
- Manufacturer
- The Procter & Gamble Manufacturing Company
- Effective date
- 2026-10-05
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 12
- Source
- daily-update
- Hydrated at
- 2026-10-07 01:02:58
Label at a glance#
ProductVicks NyQuil HIGH BLOOD PRESSURE Cold and Flu
Active ingredientACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
Label structure12 sections
Dosage and administration
take only as directed only use the dose cup provided do not exceed 4 doses per 24 hrs adults & children 12 yrs & over 30 mL per dose every 6 hrs children 4 to under 12 yrs ask a doctor children under 4 yrs do not use
Storage and handling
each 30 mL contains: sodium 28.23 mg store at no greater than 25°C and do not refrigerate
Contacts and useful links#
Label contents#
Full prescribing information#
SPL UNCLASSIFIED SECTION
Drug Facts
Active ingredients (in each 30 mL)
Acetaminophen 650 mg
Dextromethorphan HBr 30 mg
Doxylamine succinate 12.5 mg
Purpose
Pain reliever/fever reducer
Cough suppressant
Antihistamine
Uses
temporarily relieves common cold/flu symptoms:
- cough due to minor throat and bronchial irritation
- sore throat
- headache
- minor aches and pains
- fever
- runny nose and sneezing
Warnings
Liver warning:
This product contains acetaminophen.
Severe liver damage may occur if you take
• more than 4 doses (30 mL each dose) in 24 hours, which is the maximum daily amount for this product
• with other drugs containing acetaminophen
• 3 or more alcoholic drinks every day 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
- glaucoma
- cough that occurs with too much phlegm (mucus)
- a breathing problem or chronic cough that lasts or as occurs with smoking, asthma, chronic bronchitis or emphysema
- trouble urinating due to enlarged prostate gland
Ask a doctor or pharmacist before use if you are
- taking sedatives or tranquilizers
- taking the blood thinning drug warfarin
When using this product
- excitability may occur, especially in children
- marked drowsiness may occur
- avoid alcoholic drinks
- be careful when driving a motor vehicle or operating machinery
- alcohol, sedatives, and tranquilizers may increase drowsiness
Stop use and ask a doctor if
- pain 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.
OTC - PREGNANCY OR BREAST FEEDING SECTION
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
- only use the dose cup provided
- do not exceed 4 doses per 24 hrs
| adults & children 12 yrs & over | 30 mL per dose every 6 hrs |
| children 4 to under 12 yrs | ask a doctor |
| children under 4 yrs | do not use |
Other information
- each 30 mL contains: sodium 28.23 mg
- store at no greater than 25°C and do not refrigerate
Inactive ingredients
citric acid, FD&C blue no. 1, FD&C red no. 40, flavor, glycerin, propylene glycol, saccharin sodium, sodium benzoate, sodium citrate, sorbitol, sucralose, water, xanthan gum
Questions?
1-800-362-1683
SPL UNCLASSIFIED SECTION
TAMPER EVIDENT: Do not use if printed shrinkband seal around the neck is broken or missing
SPL UNCLASSIFIED SECTION
DIST. BY:
PROCTER & GAMBLE
CINCINNATI, OH 45202
PRINCIPAL DISPLAY PANEL - 236 ml Bottle Label
VICKS ®
NyQuil ™
HIGH BLOOD PRESSURE
COLD & FLU
Acetaminophen, Doxylamine Succinate, Dextromethorphan HBr
Headache, Fever, Sore Throat, Minor Aches & Pains
Sneezing, Runny Nose
Cough
SUGAR & ALCOHOL FREE
Nighttime Relief
DECONGESTANT FREE
8 FL OZ (236 mL)
Product Linked Resources#
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 59361619-24d9-b610-eca6-5a7f25ed5e03 | Product name | 5 | 20240909 |
| f4368033-af8c-41bf-a84b-ff77392b8522 | Product name | 1 | 20161229 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 69423-973-06 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1296-111a-e063-dadaa90a10e2 | VICKS ® NyQuil™ HIGH BLOOD PRESSURE COLD & FLU |
| 69423-973-06 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1296-111a-e063-dadaa90a10e2 | VICKS ® NyQuil™ HIGH BLOOD PRESSURE COLD & FLU |
| 69423-973-08 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1296-111a-e063-dadaa90a10e2 | VICKS ® NyQuil™ HIGH BLOOD PRESSURE COLD & FLU |
| 69423-973-08 | 2024-01-30 | C162847 | 48780-1 | 1030e365-1296-111a-e063-dadaa90a10e2 | VICKS ® NyQuil™ HIGH BLOOD PRESSURE COLD & FLU |
Products#
Every source-derived product name is available through these pages.
- Vicks NyQuil HIGH BLOOD PRESSURE Cold and Flu
- Acetaminophen, Dextromethorphan Hydrobromide, and Doxylamine succinate
- ACETAMINOPHEN
- DEXTROMETHORPHAN HYDROBROMIDE
- DEXTROMETHORPHAN
- DOXYLAMINE SUCCINATE
- DOXYLAMINE
- FD&C BLUE NO. 1
- FD&C RED NO. 40
- PROPYLENE GLYCOL
- WATER
- SACCHARIN SODIUM
- SODIUM CITRATE
- SODIUM BENZOATE
- SUCRALOSE
- SORBITOL
- XANTHAN GUM
- GLYCERIN
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 69423-973 | 69423-973-06, 69423-973-08 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ACETAMINOPHEN | 362O9ITL9D | ACTIB |
| DEXTROMETHORPHAN HYDROBROMIDE | 9D2RTI9KYH | ACTIB |
| DOXYLAMINE SUCCINATE | V9BI9B5YI2 | ACTIB |
| FD&C BLUE NO. 1 | H3R47K3TBD | IACT |
| FD&C RED NO. 40 | WZB9127XOA | IACT |
| PROPYLENE GLYCOL | 6DC9Q167V3 | IACT |
| WATER | 059QF0KO0R | IACT |
| SACCHARIN SODIUM | SB8ZUX40TY | IACT |
| SODIUM CITRATE | 1Q73Q2JULR | IACT |
| SODIUM BENZOATE | OJ245FE5EU | IACT |
| SUCRALOSE | 96K6UQ3ZD4 | IACT |
| SORBITOL | 506T60A25R | IACT |
| XANTHAN GUM | TTV12P4NEE | IACT |
| GLYCERIN | PDC6A3C0OX | IACT |
Source Document#
Older Hydrated Versions#
| Version | Effective date | Source | Hydrated |
|---|---|---|---|
| 11 | 2025-12-01 | full-release | 2026-06-01 01:18:59 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 44e86d7c-7ff2-5a1f-e063-6294a90a0495 | d83c4691-785d-d1a0-e053-2995a90ad196 | 2025-12-01 | Warnings | d83c4691-785d-d1a0-e053-2995a90ad196 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.