Label: ALAVERT ALLERGY- loratadine tablet, orally disintegrating
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NDC Code(s):
0573-2620-01,
0573-2620-19,
0573-2620-65,
0573-2620-71, view more0573-2621-13, 0573-2621-19, 0573-2621-65
- Packager: Haleon US Holdings LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: New Drug Application
Drug Label Information
Updated March 21, 2024
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- 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 use more than directed. Taking more than recommended may cause drowsiness.
- DIRECTIONS
- OTHER INFORMATION
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INACTIVE INGREDIENTS
Alavert Allergy Fresh Mint
anhydrous citric acid, aspartame, colloidal silicon dioxide, corn syrup solids, crospovidone, magnesium stearate, mannitol, microcrystalline cellulose, modified starch, natural and artificial flavors, sodium bicarbonate
Alavert Allergy Citrus Burst
anhydrous citric acid, aspartame, butylated hydroxyanisole, colloidal silicon dioxide, corn syrup solids, crospovidone, dextrin, ferric oxides, magnesium stearate, maltodextrin, mannitol, microcrystalline cellulose, modified starch, natural and artificial flavors, sodium bicarbonate
- QUESTIONS OR COMMENTS?
-
PRINCIPAL DISPLAY PANEL
The product packaging shown below represents a sample of that currently in use. Additional packaging may also be available.
ALAVERT allergy Fresh Mint
Loratadine Orally Disintegrating Tablet, 10 mg, Antihistamine
18 Orally Disintegrating Tablets
TASTES GREAT!
Melts in your Mouth!
Non-Drowsy* Allergy Relief
*When taken as directed. See Drug Facts Panel.
24 HOUR Relief of
- Sneezing
- Runny Nose
- Itchy, Watery Eyes
- Itching of Nose & Throat
Compare to Claritin †& SAVE!
†Claritin is a registered trademark of Schering Corporation
-
PRINCIPAL DISPLAY PANEL
ALAVERT allergy Citrus Burst
Loratadine Orally Disintegrating Tablet, 10 mg, Antihistamine
18 Orally Disintegrating Tablets
TASTES GREAT!
Melts in your Mouth!
Non-Drowsy* Allergy Relief
*When taken as directed. See Drug Facts Panel.
24 HOUR Relief of
- Sneezing
- Runny Nose
- Itchy, Watery Eyes
- Itching of Nose & Throat
Compare to Claritin† & SAVE!
†Claritin is a registered trademark of Schering Corporation
-
INGREDIENTS AND APPEARANCE
ALAVERT ALLERGY
loratadine tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-2620 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) ASPARTAME (UNII: Z0H242BBR1) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CORN SYRUP (UNII: 9G5L16BK6N) MAGNESIUM STEARATE (UNII: 70097M6I30) MANNITOL (UNII: 3OWL53L36A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Product Characteristics Color white (off white) Score no score Shape ROUND (beveled tablet) Size 14mm Flavor MINT Imprint Code A;24 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-2620-19 18 in 1 CARTON 12/19/2002 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0573-2620-01 50 in 1 BOX 12/19/2002 2 1 in 1 POUCH; Type 0: Not a Combination Product 3 NDC:0573-2620-65 60 in 1 CARTON 12/19/2002 3 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 4 NDC:0573-2620-71 1500 in 1 BOX 12/19/2002 4 1 in 1 POUCH; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date NDA NDA021375 12/19/2002 ALAVERT ALLERGY
loratadine tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:0573-2621 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg Inactive Ingredients Ingredient Name Strength ANHYDROUS CITRIC ACID (UNII: XF417D3PSL) ASPARTAME (UNII: Z0H242BBR1) BUTYLATED HYDROXYANISOLE (UNII: REK4960K2U) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) CORN SYRUP (UNII: 9G5L16BK6N) CROSPOVIDONE (120 .MU.M) (UNII: 68401960MK) ICODEXTRIN (UNII: 2NX48Z0A9G) FERRIC OXIDE RED (UNII: 1K09F3G675) MAGNESIUM STEARATE (UNII: 70097M6I30) MALTODEXTRIN (UNII: 7CVR7L4A2D) MANNITOL (UNII: 3OWL53L36A) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) SODIUM BICARBONATE (UNII: 8MDF5V39QO) Product Characteristics Color orange (an orange flat faced tablet) Score no score Shape ROUND (beveled tablet) Size 14mm Flavor CITRUS (orange mint) Imprint Code A;24 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:0573-2621-65 60 in 1 CARTON 12/19/2002 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:0573-2621-19 18 in 1 CARTON 12/19/2002 2 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 3 NDC:0573-2621-13 12 in 1 CARTON 12/19/2016 3 1 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 NDA NDA021375 12/19/2002 Labeler - Haleon US Holdings LLC (079944263)