Label: LEADER ALLERGY RELIEF- loratadine tablet
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NDC Code(s):
70000-0213-1,
70000-0213-2,
70000-0213-3,
70000-0213-4, view more70000-0213-5, 70000-0213-6
- Packager: Cardinal Health 110, LLC. dba Leader
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 23, 2021
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
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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
- Other information
- Inactive ingredients
- Questions or comments?
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Principal Display Panel
Non-Drowsy* | 24 Hour
Allergy Relief
Loratadine Tablets, 10 mg | Antihistamine
Indoor & Outdoor Allergies
24 Hour Relief of:
Sneezing; Runny Nose;
Itchy, Watery Eyes;
Itchy Throat or Nose
COMPARE TO CLARITIN
active ingredient
Original Prescription Strength
100% Money Back Guarantee
300 TABLETS
Actual Size
*When taken as directed.
See Drug Facts Panel.
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INGREDIENTS AND APPEARANCE
LEADER ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70000-0213 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 LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POVIDONE, UNSPECIFIED (UNII: FZ989GH94E) Product Characteristics Color WHITE Score no score Shape OVAL Size 8mm Flavor Imprint Code L612 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70000-0213-2 30 in 1 CARTON 12/09/2016 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:70000-0213-3 1 in 1 CARTON 12/09/2016 2 70 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:70000-0213-4 1 in 1 CARTON 12/09/2016 3 90 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:70000-0213-1 10 in 1 CARTON 12/09/2016 4 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 5 NDC:70000-0213-5 40 in 1 CARTON 12/13/2017 5 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 6 NDC:70000-0213-6 1 in 1 CARTON 01/14/2020 6 300 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 ANDA076301 12/09/2016 Labeler - Cardinal Health 110, LLC. dba Leader (063997360)