Label: NON DROWSY ALLERGY RELIEF- loratadine tablet, orally disintegrating
- NDC Code(s): 41250-890-65
- Packager: Meijer Distribution Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated September 28, 2020
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- 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.
- Keep out of reach of children.
- Directions
- Other information
- Inactive ingredients
- Questions or comments?
-
Package/Label Principal Display Panel
Compare to Claritin® RediTabs® active ingredient
NON-DROWSY*
allergy relief
Loratadine Orally Disintegrating Tablets, 10 mg
Antihistamine
INDOOR & OUTDOOR ALLERGIES
24 HOUR RELIEF OF:
Sneezing;
Runny Nose;
Itchy, Watery Eyes;
Itchy Throat or Nose
30 Tablets
actual size
ORIGINAL PRESCRIPTION STRENGTH
*When taken as directed. See Drug Facts Panel.
NO WATER NEEDED MELTS IN YOUR MOUTH
-
INGREDIENTS AND APPEARANCE
NON DROWSY ALLERGY RELIEF
loratadine tablet, orally disintegratingProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41250-890 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 CROSCARMELLOSE SODIUM (UNII: M28OL1HH48) CROSPOVIDONE (15 MPA.S AT 5%) (UNII: 68401960MK) HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO) MAGNESIUM STEARATE (UNII: 70097M6I30) MANNITOL (UNII: 3OWL53L36A) MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U) SUCRALOSE (UNII: 96K6UQ3ZD4) Product Characteristics Color WHITE Score no score Shape ROUND Size 6mm Flavor Imprint Code L;L Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41250-890-65 30 in 1 CARTON 09/23/2020 1 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 ANDA ANDA076011 09/23/2020 Labeler - Meijer Distribution Inc (006959555)