WALGREENS

Manufacturer
WALGREENS CO.
Effective date
2026-02-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:47:59

Label at a glance#

ProductWALGREENS NIGHTTIME ALLERGY RELIEF
Active ingredientDOXYLAMINE SUCCINATE
Label structure16 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 only use the dose cup provided do not exceed 4 doses per 24 hrs adults & children 12 yrs & over 30 mL every 4 hrs children 6 to under 12 yrs 15 mL every 4 hrs children 4 to under 6 yrs ask a doctor children under 4 yrs do not use

Storage and handling

each 15 mL contains: sodium 15 mg Store at room temperature

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient (in each 15 mL)

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

Ask a doctor before use if you have

OTC - ASK DOCTOR SECTION

  • 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

Ask a doctor or pharmacist before use if you are

OTC - ASK DOCTOR/PHARMACIST SECTION

  • 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

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

OVERDOSAGE SECTION

In case of overdose, get medical help or contact a Poison Control Center right away at 1-800-222-1222. 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
  • only use the dose cup provided
  • do not exceed 4 doses per 24 hrs

adults & children 12 yrs & over

30 mL every 4 hrs

children 6 to under 12 yrs

15 mL every 4 hrs

children 4 to under 6 yrs

ask a doctor

children under 4 yrs

do not use

Other information

STORAGE AND HANDLING SECTION

  • each 15 mL contains:sodium 15 mg
  • Store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

citric acid, FD&C Red No. 40, flavor, glycerin, poloxamer, propylene glycol, glycol, purified water, sodium benzoate, sodium citrate, sorbitol, sucralose, xanthan gum

Questions or comments?

OTC - QUESTIONS SECTION

1-866-467-2748

SPL UNCLASSIFIED SECTION

TAMPER EVIDENT: DO NOT USE IF IMPRINTED SHRINKBAND IS MISSING OR BROKEN.

SPL UNCLASSIFIED SECTION

Distributed by:

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Compare to the active ingredient in Vicks® NyQuil™ Allergy*

NDC 0363-6251-24

Nighttime

Allergy Relief

Doxylamine Succinate -Antihistamine

  • Runny Nose
  • Sneezing
  • Itchy, Watery Eyes
  • Itchy Throat and Nose

Mixed Berry Flavor

Naturally and Artificially Flavored

2 BOTTLES -12 FL OZ (354 mL) EACH; TOTAL 24 FL OZ(708 ML)

*This product is not manufactured or distributed by Procter & Gamble, the distributor of Vicks® NyQuil™ Allergy.

WAG Nighttime Allergy Relief Twin Pack 708ML
WAG Nighttime Allergy Relief Twin Pack 708ML

Package Label of 354 mL

SPL UNCLASSIFIED SECTION

WAG Nighttime Allergy Relief 12FL OZ 354 mL
WAG Nighttime Allergy Relief 12FL OZ 354 mL

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2715412doxylamine succinate 6.25 MG in 15 mL Oral SolutionPSN1
2715412doxylamine succinate 0.417 MG/ML Oral SolutionSCD1
2715412doxylamine succinate 6.25 MG per 15 ML Oral SolutionSY1

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
DOXYLAMINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130000000000000GTIN-13: 0000000000000
EAN-13: 0000000000000
GTIN-12: 000000000000
UPC-A: 000000000000
GTIN storage (14 digits): 00000000000000
346.jpg, 625MB12WAG.jpg

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
59361619-24d9-b610-eca6-5a7f25ed5e03Product name520240909
f4368033-af8c-41bf-a84b-ff77392b8522Product name120161229

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-6251-12WALGREENSNIGHTTIME ALLERGY RELIEF354 mL in 1 BOTTLE, PLASTICLIQUID3541
0363-6251-24WALGREENSNIGHTTIME ALLERGY RELIEF354 mL in 1 BOTTLE, PLASTICLIQUID3541
0363-6251-24WALGREENSNIGHTTIME ALLERGY RELIEF2 in 1 CARTONLIQUID21

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
0363-62510363-6251-12, 0363-6251-24

Ingredients#

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

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

Source Document#

Source XML

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
WALGREENS NIGHTTIME ALLERGY RELIEFDOXYLAMINE SUCCINATEWALGREENS CO.a3c7df98-4611-4b61-9c03-5e687364bf742026-02-27WarningsExact identifier
ndc (package): 0363-6251-24
ndc (package): 0363-6251-12
ndc (product): 0363-6251
ndc11 (package): 00363625124
ndc11 (package): 00363625112
spl id: 4bd9e9b4-1205-8f35-e063-6294a90acc84
spl set id: a3c7df98-4611-4b61-9c03-5e687364bf74

Reported adverse events (FAERS/openFDA)#

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