Label: CAREONE CHILDRENS ALLERGY RELIEF- cetirizine hcl solution
- NDC Code(s): 41520-301-26
- Packager: American Sales Company
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 21, 2019
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- Official Label (Printer Friendly)
- 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
Compare to the active ingredient in Children’s Zyrtec®
For Ages 2 Years and Older
Children’s Allergy Relief
Cetirizine Hydrochloride Oral Solution 1 mg/mL Antihistamine
dosing cup included
Bubble Gum Flavored
24-HOUR RELIEF OF:
Itchy, Watery Eyes
Itchy Throat or Nose
Indoor & Outdoor Allergies
OUR PHARMACISTS RECOMMEND
4 FL OZ (118mL)
INGREDIENTS AND APPEARANCE
CAREONE CHILDRENS ALLERGY RELIEF
cetirizine hcl solution
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41520-301 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:41520-301-26 1 in 1 CARTON 10/09/2017 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 04/06/2016 Labeler - American Sales Company (809183973)