Label: WAL-ITIN- loratadine tablet, chewable
- NDC Code(s): 0363-0754-30
- Packager: Walgreens
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated July 29, 2019
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- Active ingredient (in each tablet)
- 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
- chew or crush tablets completely before swallowing.
adults and children
6 years and overchew 2 tablets daily; not more
than 2 tablets in 24 hourschildren 2 to under
6 years of agechew 1 tablet daily; not more
than 1 tablet in 24 hourschildren under
2 years of ageask a doctor consumers with liver
or kidney diseaseask a doctor - Other information
- Inactive ingredients
- Questions?
- SPL UNCLASSIFIED SECTION
-
PRINCIPAL DISPLAY PANEL - 5 mg Tablet Blister Pack Carton
children's
ALLERGYWal-itin®
LORATADINE CHEWABLE TABLETS USP, 5 mg / ANTIHISTAMINEWalgreens
Compare to Children's Claritin®
Chewables active ingredient††NDC 0363-0754-30
NEW
CHEWABLE
NON-DROWSY*
24-HOUR RELIEF- 24-hour relief of sneezing, runny nose,
itchy throat or nose, & itchy, watery eyes - Indoor & outdoor allergies
30
CHEWABLE
TABLETSThe chewable tablets are to be chewed before swallowing.
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.
BUBBLEGUM
FLAVORACTUAL SIZE
AGES
2
YEARS &
OLDER - 24-hour relief of sneezing, runny nose,
-
INGREDIENTS AND APPEARANCE
WAL-ITIN
loratadine tablet, chewableProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0363-0754 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 5 mg Inactive Ingredients Ingredient Name Strength aspartame (UNII: Z0H242BBR1) COCHINEAL (UNII: TZ8Z31B35M) ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) magnesium stearate (UNII: 70097M6I30) mannitol (UNII: 3OWL53L36A) microcrystalline cellulose (UNII: OP1R32D61U) SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2) stearic acid (UNII: 4ELV7Z65AP) Product Characteristics Color PINK (light to medium pink with a slightly speckled appearance) Score no score Shape ROUND (Flat face, beveled edge) Size 10mm Flavor BUBBLE GUM Imprint Code 754 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0363-0754-30 3 in 1 CARTON 03/01/2018 1 10 in 1 BLISTER PACK; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA210088 03/01/2018 Labeler - Walgreens (008965063) Registrant - Ohm Laboratories (184769029) Establishment Name Address ID/FEI Business Operations Ohm Laboratories 184769029 MANUFACTURE(0363-0754)