dye-free children's allergy relief
322d9a03-a908-4858-b25e-6eba2411fa03
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Purpose
Antihistamine
Description
Drug Facts
Medication Information
Active Ingredient
Loratadine USP, 5 mg
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
-
•runny nose
-
•sneezing
-
•itchy, watery eyes
-
•itching of the nose or throat
Purpose
Antihistamine
Directions
-
•chew or crush tablets completely before swallowing.
|
adults and children 6 years and over |
chew 2 tablets daily; not more than 2 tablets in 24 hours |
|
children 2 to under 6 years of age |
chew 1 tablet daily; not more than 1 tablet in 24 hours |
|
children under 2 years of age |
ask a doctor |
|
consumers with liver or kidney disease |
ask a doctor |
Other Information
-
•phenylketonurics: contains phenylalanine 1.25 mg per tablet.
-
•TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
-
•store between 20° to 25°C (68° to 77°F).
Inactive Ingredients
aspartame, citric acid anhydrous, colloidal silicon dioxide, flavor, magnesium stearate, mannitol, microcrystalline cellulose, sodium starch glycolate, stearic acid
Description
Drug Facts
Questions?
call toll-free Monday to Friday 8:30 am to 5:00 pm EST at 1-800-406-7984.
Keep the carton. It contains important information. See end panel for expiration date.
Section 42229-5
Drug Facts
Section 50565-1
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Section 50566-9
Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
Section 50567-7
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
Section 50569-3
Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
Section 50570-1
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Section 53414-9
If pregnant or breast-feeding, ask a health professional before use.
Principal Display Panel 30 Tablet Blister Pack Carton
Structured Label Content
Active Ingredient (Active ingredient (in each tablet))
Loratadine USP, 5 mg
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
-
•runny nose
-
•sneezing
-
•itchy, watery eyes
-
•itching of the nose or throat
Purpose
Antihistamine
Directions
-
•chew or crush tablets completely before swallowing.
|
adults and children 6 years and over |
chew 2 tablets daily; not more than 2 tablets in 24 hours |
|
children 2 to under 6 years of age |
chew 1 tablet daily; not more than 1 tablet in 24 hours |
|
children under 2 years of age |
ask a doctor |
|
consumers with liver or kidney disease |
ask a doctor |
Other Information (Other information)
-
•phenylketonurics: contains phenylalanine 1.25 mg per tablet.
-
•TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
-
•store between 20° to 25°C (68° to 77°F).
Inactive Ingredients (Inactive ingredients)
aspartame, citric acid anhydrous, colloidal silicon dioxide, flavor, magnesium stearate, mannitol, microcrystalline cellulose, sodium starch glycolate, stearic acid
Questions?
call toll-free Monday to Friday 8:30 am to 5:00 pm EST at 1-800-406-7984.
Keep the carton. It contains important information. See end panel for expiration date.
Section 42229-5 (42229-5)
Drug Facts
Section 50565-1 (50565-1)
Keep out of reach of children.
In case of overdose, get medical help or contact a Poison Control Center right away (1-800-222-1222).
Section 50566-9 (50566-9)
Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
Section 50567-7 (50567-7)
When using this product do not take more than directed. Taking more than directed may cause drowsiness.
Section 50569-3 (50569-3)
Ask a doctor before use if you have liver or kidney disease. Your doctor should determine if you need a different dose.
Section 50570-1 (50570-1)
Do not use if you have ever had an allergic reaction to this product or any of its ingredients.
Section 53414-9 (53414-9)
If pregnant or breast-feeding, ask a health professional before use.
Principal Display Panel 30 Tablet Blister Pack Carton (PRINCIPAL DISPLAY PANEL - 30 Tablet Blister Pack Carton)
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:00:14.657641 · Updated: 2026-03-14T23:00:37.728626