Label: EQUALINE ALLERGY RELIEF- loratadine tablet
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NDC Code(s):
41163-612-46,
41163-612-58,
41163-612-60,
41163-612-65, view more41163-612-72, 41163-612-75, 41163-612-95
- Packager: United Natural Foods, Inc. dba UNFI
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated July 24, 2023
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
compare to Claritin® Tablets active ingredient
allergy relief
loratadine tablets, 10mg (antihistamine)
non-drowsy*
indoor & outdoor allergies
24 hour relief of:
sneezing
runny nose
itchy, watery eyes
itchy throat or nose
*WHEN TAKEN AS DIRECTED. SEE DRUG FACTS PANEL.
30 tablets
30 days of relief
actual size
ORIGINAL PRESCRIPTION STRENGTH
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INGREDIENTS AND APPEARANCE
EQUALINE ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-612 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:41163-612-46 10 in 1 CARTON 02/07/2005 1 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 2 NDC:41163-612-65 1 in 1 CARTON 02/15/2005 2 30 in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:41163-612-72 1 in 1 CARTON 03/23/2005 3 60 in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:41163-612-75 1 in 1 CARTON 03/21/2005 4 90 in 1 BOTTLE; Type 0: Not a Combination Product 5 NDC:41163-612-60 20 in 1 CARTON 02/08/2005 11/11/2011 5 1 in 1 BLISTER PACK; Type 0: Not a Combination Product 6 NDC:41163-612-95 1 in 1 CARTON 08/31/2009 06/17/2012 6 45 in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:41163-612-58 1 in 1 CARTON 10/03/2019 12/31/2021 7 40 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 02/07/2005 Labeler - United Natural Foods, Inc. dba UNFI (943556183)