Loratadine Allergy Relief
a53e5635-8633-4c28-b04f-cdfb3d851e68
34390-5
HUMAN OTC DRUG LABEL
Drug Facts
Composition & Product
Identifiers & Packaging
Description
Drug Facts
Purpose
Antihistamine
How Supplied
Product: 50090-2387 NDC: 50090-2387-0 30 TABLET in a BLISTER PACK
Medication Information
Purpose
Antihistamine
How Supplied
Product: 50090-2387
NDC: 50090-2387-0 30 TABLET in a BLISTER PACK
Description
Drug Facts
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- sneezing
- itching of the nose or throat
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.
Directions
| 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 |
Loratadine
Questions?
call 1-800-406-7984
Other Information
- store between 20° to 25° C (68° to 77° F)
- protect from excessive moisture
- TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
Inactive Ingredients
corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch
Active Ingredient (in Each Tablet)
Loratadine, USP 10 mg
Structured Label Content
Uses
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- itchy, watery eyes
- sneezing
- itching of the nose or throat
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.
Purpose
Antihistamine
Directions
| 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 |
Loratadine
Questions?
call 1-800-406-7984
How Supplied (HOW SUPPLIED)
Product: 50090-2387
NDC: 50090-2387-0 30 TABLET in a BLISTER PACK
Other Information
- store between 20° to 25° C (68° to 77° F)
- protect from excessive moisture
- TAMPER EVIDENT: DO NOT USE IF BLISTER UNITS ARE TORN, BROKEN OR SHOW ANY SIGNS OF TAMPERING.
Inactive Ingredients (Inactive ingredients)
corn starch, lactose monohydrate, magnesium stearate, pregelatinized starch
Active Ingredient (in Each Tablet) (Active ingredient (in each tablet))
Loratadine, USP 10 mg
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:02:45.966611 · Updated: 2026-03-14T23:13:48.939099