CABINET ALL DAY ALLERGY RELIEF- cetirizine hydrochloride tablet

Cabinet All Day Allergy Relief by

Drug Labeling and Warnings

Cabinet All Day Allergy Relief by is a Otc medication manufactured, distributed, or labeled by Cabinet Health P.B.C.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredient (in each caplet)

Cetirizine HCl 10 mg

Purpose

Antihistamine

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

Warnings

Do not use

if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine

Ask a doctor before use if you have

liver or kidney disease. Your doctor should determine if you need a different dose.

Ask a doctor or pharmacist before use if you are

taking tranquilizers or sedatives

When using this product

• drowsiness may occur
• avoid alcohlic drinks
• alcohol, sedatives, and tranquilizers may increase drowsiness
• be careful when driving a motor vehicle or operating machinery

Stop use and ask a doctor if

an allergic reaction to this product occurs. Seek medical help right away.

If pregnant or breast-feeding,

• if breast-feeding: not recommended
• if pregnant: 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. (1-800-222-1222)

Directions

• adults and children 6 years of age and over:
  • one 10 mg caplet once daily; do not take more than one 10 mg caplet in 24 hours. A 5 mg product may be appropriate for less severe symptoms.
• adults 65 years and over:
  • ask a doctor
• children under 6 years of age:
  • ask a doctor
• consumers with liver or kidney disease:
  • ask a doctor

Other information

• store between 20° and 25°C (68° and 77°F)
• avoid high humidity and excessive heat above 40°C (104°F)
• protect from light
• contains no ingredient made from a gluten-containing grain (wheat, barley or rye)

Inactive ingredients

hypromellose, lactose, magnesium stearate, maize starch, polyethylene glycol, povidone, titanium dioxide

Questions?

call 1-908-242-6108 Mon-Fri 8:00 AM to 5:00 PM EST

Package Labeling:

INGREDIENTS AND APPEARANCE

CABINET ALL DAY ALLERGY RELIEF 
cetirizine hydrochloride tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 82725-3103
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24)	CETIRIZINE	10 mg

Inactive Ingredients
Ingredient Name	Strength
HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, CORN (UNII: O8232NY3SJ)
POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
POVIDONE (UNII: FZ989GH94E)
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)

Product Characteristics
Color	white	Score	no score
Shape	BULLET	Size	8mm
Flavor		Imprint Code	CTN;10
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 82725-3103-3	300 in 1 BOTTLE; Type 0: Not a Combination Product	03/21/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA077829	03/21/2025

Labeler - Cabinet Health P.B.C. (117102391)