FDA.reportPublic FDA data

Vicks NyQuil Allergy

Manufacturer
The Procter & Gamble Manufacturing Company
Effective date
2026-10-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
daily-update
Hydrated at
2026-10-13 04:05:26

Label at a glance#

ProductVicks NyQuil Allergy
Active ingredientDOXYLAMINE SUCCINATE
Label structure12 sections

Indications and uses

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: runny nose sneezing itchy, watery eyes itching of the nose or throat

Dosage and administration

take only as directed do not exceed 4 doses (8 LiquiCaps) per 24 hrs  adults & children 12 yrs & over  2 LiquiCaps every 4 hrs  children 4 to under 12 yrs     ask a doctor  children under 4 yrs     do not use

Storage and handling

store at no greater than 25°C (77°F)

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients (in each LiquiCap)

OTC - ACTIVE INGREDIENT SECTION

Doxylamine succinate 6.25 mg

Purpose

OTC - PURPOSE SECTION

Antihistamine

Uses

INDICATIONS & USAGE SECTION

temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:

  • runny nose
  • sneezing
  • itchy, watery eyes
  • itching of the nose or throat

Warnings

WARNINGS SECTION

OTC - ASK DOCTOR SECTION

Ask a doctor before use if you have

  • glaucoma
  • trouble urinating due to enlarged prostate gland 
  • cough that occurs with too much phlegm (mucus)
  • a breathing problem that lasts or occurs with chronic bronchitis or emphysema

OTC - ASK DOCTOR/PHARMACIST SECTION

Ask a doctor or pharmacist before use if you are

  • taking sedatives or tranquilizers

When using this product

OTC - WHEN USING SECTION

  • excitability may occur, especially in children
  • marked drowsiness may occur
  • alcohol, sedatives, and tranquilizers may increase drowsiness
  • avoid alcoholic drinks
  • be careful when driving a motor vehicle or operating machinery

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

OVERDOSAGE SECTION

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

DOSAGE & ADMINISTRATION SECTION

  • take only as directed
  • do not exceed 4 doses (8 LiquiCaps) per 24 hrs
 adults & children 12 yrs & over 2 LiquiCaps every 4 hrs
 children 4 to under 12 yrs    ask a doctor
 children under 4 yrs    do not use

Other information

STORAGE AND HANDLING SECTION

  • store at no greater than 25°C (77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

1,4-sorbitan, ascorbic acid, D&C Red No.33, gelatin, glycerin, mannitol, polyethylene glycol 400, povidone, propylene glycol, sorbitol, water

Questions?

OTC - QUESTIONS SECTION

1-800-362-1683

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: DO NOT USE IF BLISTER IS OPENED OR TORN. IF DIFFICULT TO OPEN, USE SCISSORS.

SPL UNCLASSIFIED SECTION

MADE IN CANADA

DIST. BY PROCTER & GAMBLE

CINCINNATI OH 45202.

PRINCIPAL DISPLAY PANEL - 24 LIQUICAPS

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

VICKS

NyQuil

ALLERGY

Doxylamine Succinate - Antihistamine

Runny Nose

Sneezing

Itchy, Watery Eyes

Itchy Throat and Nose

24 LIQUICAPS

381381

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codescan.pg.com/01/00323900048973381.jpg
Data codeData Matrix21500150381.jpg

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
84126-38184126-381-24

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Name, UNII, Kind table
NameUNIIKind
DOXYLAMINE SUCCINATEV9BI9B5YI2ACTIB
POVIDONEFZ989GH94EIACT
1,4-SORBITANAV0YTZ4E6JIACT
ASCORBIC ACIDPQ6CK8PD0RIACT
D&C RED NO. 339DBA0SBB0LIACT
GELATIN2G86QN327LIACT
GLYCERINPDC6A3C0OXIACT
MANNITOL3OWL53L36AIACT
POLYETHYLENE GLYCOL 400B697894SGQIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
SORBITOL506T60A25RIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12026-07-01weekly-update2026-07-17 21:42:12

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
559149b6-5082-e0ee-e063-6394a90a38a5559149ac-1784-c677-e063-6294a90a06732026-07-01WarningsExact identifier
spl set id: 559149ac-1784-c677-e063-6294a90a0673

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.