Dayclear Allergy Relief

Manufacturer
GM Pharmaceuticals INC
Effective date
2023-11-27
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 21:20:07

Label at a glance#

ProductDayclear Allergy Relief
Active ingredientPYRILAMINE MALEATE, CHLOPHEDIANOL HYDROCHLORIDE
Label structure17 sections

Storage and handling

▪ store at 68 to 86°F (20 to 30°C). ▪ avoid excessive heat and humidity

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Dayclear allergy releif 8oz

OTC - ACTIVE INGREDIENT SECTION

Active Purpose
ingredients
(in each 30 mL)
Chlophedianol Cough
HCl 25 mg ............... suppressant
Pyrilamine Maleate
50 mg .................... Antihistamine

INDICATIONS & USAGE SECTION

temporarily relieves these
symptoms due to the common
cold, hay fever (allergic rhinitis) or
other upper respiratory allergies:
▪ cough due to minor throat and
bronchial irritation
▪ runny nose
▪ sneezing
▪ itching of the nose or throat
▪ itchy, watery eyes

WARNINGS AND PRECAUTIONS SECTION

Do not exceed recommended
dosage.

OTC - ASK DOCTOR SECTION

▪ a cough that lasts or is chronic
such as occurs with smoking,
asthma, or emphysema
▪ a cough that occurs with too
much phlegm (mucus)
▪ glaucoma

▪ a breathing problem such
as emphysema or chronic
bronchitis
▪ difficulty in urination due
to enlargement of the
prostate gland

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.

DOSAGE & ADMINISTRATION SECTION

▪ do not exceed
recommended dosage.
▪ do not take more than 4
doses in any 24-hour
period.
▪ use enclosed dose cup
▪ keep dosage cup with
product
▪ mL = milliliter
▪ adults and children 12
years and over: 30 mL
every 6-8 hours
▪ children under 12: do
not use

OTHER SAFETY INFORMATION

each 30 mL contains:
Sodium 17 mg.
▪ tamper evident: Do not
use if foil seal under cap
is broken or missing.
▪ read all product
information before
using.

STORAGE AND HANDLING SECTION

▪ store at 68 to 86°F
(20 to 30°C).
▪ avoid excessive heat
and humidity

INACTIVE INGREDIENT SECTION

citric acid, glycerin, propylene glycol, purified water, sodium benzoate, sodium citrate, sodium saccharin, sorbitol

OTC - QUESTIONS SECTION

Call 1-888-535-0305

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children.

WARNINGS SECTION

Do not exceed recommended dosage

OTC - PURPOSE SECTION

temporarily relieves these
symptoms due to the common
cold, hay fever (allergic rhinitis) or
other upper respiratory allergies:
▪ cough due to minor throat and
bronchial irritation
▪ runny nose
▪ sneezing
▪ itching of the nose or throat
▪ itchy, watery eyes

RECENT MAJOR CHANGES SECTION

Indications and usage

Keep out of reach of children

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal display label

Dayclear allergy releif 8oz

NDC 58809-211-08

princpal display labelprincpal display label

princpal display label-2princpal display label-2princpal display label-3princpal display label-3

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
58809-21158809-211-08

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
0b27559c-8839-b387-e063-6394a90a0a74dfd95067-68c0-8bcd-e053-2995a90a92722023-11-27WarningsExact identifier
spl id: 0b27559c-8839-b387-e063-6394a90a0a74
spl set id: dfd95067-68c0-8bcd-e053-2995a90a9272

Reported adverse events (FAERS/openFDA)#

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