DAYCLEAR ALLERGY RELIEF- allergy releif liquid

Dayclear Allergy Relief by

Drug Labeling and Warnings

Dayclear Allergy Relief by is a Otc medication manufactured, distributed, or labeled by GM Pharmaceuticals INC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Dayclear allergy releif 8oz

ACTIVE INGREDIENT

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

INDICATIONS & USAGE

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

Do not exceed recommended
dosage.

ASK DOCTOR

▪ 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

PREGNANCY OR BREAST FEEDING

ask a
health professional
before use.

OVERDOSAGE

In case of overdose, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION

▪ 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

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

INACTIVE INGREDIENT

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

QUESTIONS

Call 1-888-535-0305

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children.

WARNINGS

Do not exceed recommended dosage

PURPOSE

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

PRINCIPAL DISPLAY PANEL

Principal display label

Dayclear allergy releif 8oz

NDC: 58809-211-08

INGREDIENTS AND APPEARANCE

DAYCLEAR ALLERGY RELIEF 
allergy releif liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 58809-211
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PYRILAMINE MALEATE (UNII: R35D29L3ZA) (PYRILAMINE - UNII:HPE317O9TL)	PYRILAMINE MALEATE	50 mg  in 30 mL
CHLOPHEDIANOL HYDROCHLORIDE (UNII: 69QQ58998Y) (CHLOPHEDIANOL - UNII:42C50P12AP)	CHLOPHEDIANOL HYDROCHLORIDE	25 mg  in 30 mL

Inactive Ingredients
Ingredient Name	Strength
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
SORBITOL (UNII: 506T60A25R)
SODIUM CITRATE (UNII: 1Q73Q2JULR)
SACCHARIN SODIUM (UNII: SB8ZUX40TY)
SODIUM BENZOATE (UNII: OJ245FE5EU)
ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 58809-211-08	237 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product	07/01/2017	05/31/2024

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M012	07/01/2017	05/31/2024

Labeler - GM Pharmaceuticals INC (793000860)