Label: LORATADINE ALLERGY RELIEF- loratadine tablet
-
Contains inactivated NDC Code(s)
NDC Code(s): 67046-452-07, 67046-452-14, 67046-452-15, 67046-452-21, view more67046-452-28, 67046-452-30, 67046-452-60 - Packager: Contract Pharmacy Services-PA
- This is a repackaged label.
- Source NDC Code(s): 51660-526
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated December 26, 2018
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENT(S)
- PURPOSE
- USE(S)
-
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?
-
PRINCIPAL DISPLAY PANEL
NDC 67046-452-30
†Compare to the active ingredient of Claritin®
NON-DROWSY*
24 HourAllergy Relief
ohm®
Loratadine Tablets USP, 10 mg
Antihistamine
Indoor & Outdoor Allergies
Relief of:
- Sneezing
- Runny Nose
- Itchy, Watery Eyes
- Itchy Throat or Nose
30 Tablets
When taken as directed. See Drug Facts Panel.
Manufactured by: Ohm Laboratories Inc.
5069178/0908
-
INGREDIENTS AND APPEARANCE
LORATADINE ALLERGY RELIEF
loratadine tabletProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:67046-452(NDC:51660-526) 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 STARCH, CORN (UNII: O8232NY3SJ) LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) Product Characteristics Color white (White to Off White) Score no score Shape ROUND Size 6mm Flavor Imprint Code RX526 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:67046-452-07 7 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 2 NDC:67046-452-30 30 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 3 NDC:67046-452-60 60 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 4 NDC:67046-452-14 14 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 5 NDC:67046-452-15 15 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 6 NDC:67046-452-28 28 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 7 NDC:67046-452-21 21 in 1 BLISTER PACK; Type 0: Not a Combination Product 09/19/2017 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA076134 09/19/2017 Labeler - Contract Pharmacy Services-PA (945429777) Establishment Name Address ID/FEI Business Operations Coupler Enterprises 945429777 repack(67046-452)