Label: EQUALINE ALLERGY RELIEF NON DROWSY- loratadine tablet, orally disintegrating
- NDC Code(s): 41163-311-65
- Packager: Supervalu Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Updated July 21, 2009
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- Active ingredient (in each tablet)
Loratadine 10 mgClose
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- itching of the nose or throat
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.
Stop use and ask a doctor if
an allergic reaction to this product occurs. Seek medical help right away.
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away.
- place 1 tablet on tongue; tablet disintegrates, with or without water
adults and children 6 years and over 1 tablet daily; not more than 1 tablet in 24 hours children under 6 years of age ask a doctor consumers with liver or kidney disease ask a doctor
- Other information
- Phenylketonurics: contains Phenylalanine 0.9 mg per tablet
- do not use if blister unit is broken or torn
- store between 20° to 25°C (68° to 77°F)
- use tablet immediately after opening individual blister
- Inactive ingredients
anhydrous citric acid, artificial cherry flavor, aspartame, colloidal silicon dioxide, crospovidone, lactose monohydrate, mannitol, microcrystalline cellulose, povidone, sodium lauryl sulfate, sodium stearateClose
- Questions or comments?
- Principal Display Panel
Compare to Claritin® RediTabs® active ingredient
Melts in your mouth
Loratadine Orally Disintegrating Tablets, 10 mg
24 hour Relief of:
Itchy, Watery Eyes
Itchy Throat or Nose
For adults and children six years and older
*When taken as directed. See Drug Facts Panel.
Allergy Relief Carton
- INGREDIENTS AND APPEARANCE
EQUALINE ALLERGY RELIEF NON DROWSY
loratadine tablet, orally disintegrating
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:41163-311 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength LORATADINE (UNII: 7AJO3BO7QN) (LORATADINE - UNII:7AJO3BO7QN) LORATADINE 10 mg Product Characteristics Color WHITE (to off white) Score no score Shape ROUND Size 7mm Flavor CHERRY Imprint Code none Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:41163-311-65 3 in 1 CARTON 1 10 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA075990 08/05/2004 Labeler - Supervalu Inc (006961411)