Target Corporation Children’s Allergy Relief Drug Facts

up and up allergy relief by

Drug Labeling and Warnings

up and up allergy relief by is a Otc medication manufactured, distributed, or labeled by Sixarp, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

UP AND UP ALLERGY RELIEF- cetirizine hydrochloride solution 
Sixarp, LLC

----------

Target Corporation Children’s Allergy Relief Drug Facts

Active ingredient (in each 5 mL)

Cetirizine HCl 5 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 alcoholic 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

• use only with enclosed dosing cup
• find right dose on chart below
• mL = milliliter

• adults and children 6 years and over:

  5 mL or 10 mL once daily depending upon severity of symptoms; do not take more than 10 mL in 24 hours.

• adults 65 years and over:

  5 mL once daily; do not take more than 5 mL in 24 hours.

• children 2 to under 6 years of age:

  2.5 mL once daily. If needed, dose can be increased to a maximum of 5 mL once daily or 2.5 mL every 12 hours. Do not give more than 5 mL in 24 hours.

• children under 2 years of age:

  ask a doctor

• consumers with liver or kidney disease:

  ask a doctor

Other information

• store between 20° to 25°C (68° to 77°F)
• do not use if carton is opened, or if printed neckband is broken or missing
• see bottom panel for lot number and expiration date

Inactive ingredients

artificial cherry mint flavor, glacial acetic acid, glycerin, methylparaben, propylene glycol, propylparaben, purified water, sodium acetate, sucrose

Questions?

Call 1-888-547-7400

Package/Label Principal Display Panel

Compare to active ingredient in Children’s Zyrtec®

children’s

allergy relief

cetirizine hydrochloride oral solution 1 mg/mL

antihistamine

indoor and outdoor allergies

24 hour relief of:

sneezing

runny nose

itchy, watery eyes

itchy throat or nose

24 HOUR

dye free

dosing cup included

CHERRY FLAVOR

AGES 2+ YEARS

4 FL OZ (118 mL)

UP AND UP ALLERGY RELIEF 
cetirizine hydrochloride solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 59368-004
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24)	CETIRIZINE HYDROCHLORIDE	5 mg  in 5 mL

Inactive Ingredients
Ingredient Name	Strength
ACETIC ACID (UNII: Q40Q9N063P)
GLYCERIN (UNII: PDC6A3C0OX)
METHYLPARABEN (UNII: A2I8C7HI9T)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PROPYLPARABEN (UNII: Z8IX2SC1OH)
WATER (UNII: 059QF0KO0R)
SODIUM ACETATE (UNII: 4550K0SC9B)
SUCROSE (UNII: C151H8M554)

Product Characteristics
Color		Score
Shape		Size
Flavor	CHERRY (Mint)	Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 59368-004-01	1 in 1 CARTON	12/23/2014
1		118 mL in 1 BOTTLE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
ANDA	ANDA090254	12/23/2014

Labeler - Sixarp, LLC (016329513)

Establishment
Name	Address	ID/FEI	Business Operations
Sixarp, LLC		016329513	manufacture(59368-004) , label(59368-004)

Revised: 3/2024

Document Id: 13b8c088-51e3-196a-e063-6294a90abcc0

34390-5

Set id: 13b8cd27-5400-07ea-e063-6294a90a14d6

Version: 1

Effective Time: 20240315