ALLEXPERT 24HR ANTIHISTAMINE CETIRIZINE HYDROCHLORIDE ORAL SOLUTION- allexpert 24hr antihistamine cetirizine hydrochloride solution 
Bowong Technology (ShenZhen) Co.,Ltd

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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Active Ingredient(s)

Cetirizine HCI 5mg.(in each 5ml)

Purpose

Antihistamine

Use

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

1.ASK A DOCTOR before use if you have Iver or kidney disoaso. Your doctor should dotermine iI you need a dilferent dose.
2.ASK A DOCTOR or phamaclst belore use i you aro taking tranqulzors or sodativcs.

Do not use

if you have over had an allorgic reaclion lo ths product or any ol ils ingredients or to an anlihislamine conlaining hydroxydine
or other Piperazine derivatives .

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

if an allergic reoclion lo this product occurs. Seek medical help right away.

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

Directions

See Outer box

Other information

■store between 20* to 25C (68* to 77*F)

■see bottom panel for lot number and expiration date.

Inactive ingredients

Sodium Dihydrogen Phosphate, Dibasic
Sodium Phosphate, Sodium Benzoate,
Aspartame, purified water.

Package Label - Principal Display Panel

labellabel1

ALLEXPERT 24HR ANTIHISTAMINE CETIRIZINE HYDROCHLORIDE ORAL SOLUTION 
allexpert 24hr antihistamine cetirizine hydrochloride solution
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84264-001
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE1 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM BENZOATE (UNII: OJ245FE5EU)  
ASPARTAME (UNII: Z0H242BBR1)  
SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)  
WATER (UNII: 059QF0KO0R)  
AZITHROMYCIN SODIUM DIHYDROGEN PHOSPHATE (UNII: ADV7FS82PV)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:84264-001-01150 mL in 1 BOTTLE; Type 0: Not a Combination Product04/17/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved drug other04/17/2024
Labeler - Bowong Technology (ShenZhen) Co.,Ltd (844456666)
Establishment
NameAddressID/FEIBusiness Operations
Bowong Technology (ShenZhen) Co.,Ltd844456666manufacture(84264-001)

Revised: 4/2024
Document Id: 16420fc3-2366-f20e-e063-6294a90a7ef8
Set id: 16423890-f64a-1b02-e063-6294a90a403e
Version: 1
Effective Time: 20240417
 
Bowong Technology (ShenZhen) Co.,Ltd