Label: ALLERGY CHILDRENS- loratadine liquid
- NDC Code(s): 41250-539-04
- Packager: MEIJER, INC.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated November 1, 2022
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredient (in each 5 mL teaspoonful)
- Purpose
- Uses
-
Warnings
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,
do not take more than directed. Taking more than directed may cause drowsiness.
-
Directions
- use only with enclosed dosing cup
adults and children 6 years and over 2 teaspoonfuls (tsp) daily; do not take more than 2 teaspoonfuls (tsp) in 24 hours children 2 to under 6 years of age 1 teaspoonful (tsp) daily; do not take more than 1 teaspoonful (tsp) in 24 hours children under 2 years of age ask a doctor consumers with liver or kidney disease ask a doctor
- Other information
- Inactive ingredients
- Questions or Comments?
-
Principal Display Panel
Compare to Children's Claritin® Allergy active ingredient†
CHILDREN'S
Allergy
Loratadine Oral Solution 5 mg | 5mL
Antihistamine
24 HOUR RELIEF OF
Indoor & Outdoor Allergies
Sneezing, Runny Nose,
Itchy, Watery Eyes,
Itchy Throat or Nose
For ages 2 Years and over
Non-drowsy*
Dye free
Alcohol free
Sugar-Free
Grape Flavor
*When taken as directed See Drug Facts panel.
FL OZ (mL)
†This product is not manufactured or distributed by Bayer HealthCare LLC, distributor of Children's Claritin® Allergy.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL AROUND BOTTLE IS BROKEN OR MISSING.
DIST. BY MEIJER DISTRIBUTION, INC.
GRAND RAPIDS, MI 49544
- Product Label
-
INGREDIENTS AND APPEARANCE
ALLERGY CHILDRENS
loratadine liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-539 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 5 mg in 5 mL Inactive Ingredients Ingredient Name Strength SUCRALOSE (UNII: 96K6UQ3ZD4) BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) GLYCERIN (UNII: PDC6A3C0OX) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) WATER (UNII: 059QF0KO0R) SODIUM BENZOATE (UNII: OJ245FE5EU) Product Characteristics Color Score Shape Size Flavor GRAPE Imprint Code Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-539-04 1 in 1 BOX 02/28/2018 02/28/2025 1 120 mL in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA077421 02/28/2018 02/28/2025 Labeler - MEIJER, INC. (006959555)