Label: GOOD SENSE CHILDRENS ALL DAY ALLERGY- cetirizine hcl solution
- NDC Code(s): 0113-0189-26
- Packager: L. Perrigo Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Updated December 27, 2019
If you are a consumer or patient please visit this version.
- Active ingredient (in each 5 mL)
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.
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.
- Keep out of reach of children.
- 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
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.
2 years of age
ask a doctor
consumers with liver or kidney disease
ask a doctor
- Inactive ingredients
Package/Label Principal Display Panel
2 Yrs. & Older
Children’s All Day Allergy
Cetirizine Hydrochloride Oral Solution 1 mg/mL
24 Hour Relief of:
Itchy, Watery Eyes
Itchy Throat or Nose
Indoor & Outdoor Allergies
Dosing Cup Included
Bubble Gum Flavor
Compare to active ingredient of Children’s Zyrtec®
100% SATISFACTION GUARANTEED
4 FL OZ (118 mL)
INGREDIENTS AND APPEARANCE
GOOD SENSE CHILDRENS ALL DAY ALLERGY
cetirizine hcl solution
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0113-0189 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 ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) SORBITOL (UNII: 506T60A25R) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color YELLOW (Clear to light yellow) Score Shape Size Flavor BUBBLE GUM Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0113-0189-26 1 in 1 CARTON 01/03/2014 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 ANDA204226 01/03/2014 Labeler - L. Perrigo Company (006013346)