42c9636f-07af-44a3-8d84-c11e1b57783a
34390-5
Human OTC Drug Label
Drug Facts
Composition & Product
Identifiers & Packaging
Description
Cetirizine Hydrochloride Tablets USP 10 mg (ALLERGY RELIEF) Drug Facts
Purpose
Antihistamine
How Supplied
Product: 50090-6170 NDC: 50090-6170-0 30 TABLET in a BOTTLE / 48 in a CASE
Medication Information
Purpose
Antihistamine
How Supplied
Product: 50090-6170
NDC: 50090-6170-0 30 TABLET in a BOTTLE / 48 in a CASE
Description
Cetirizine Hydrochloride Tablets USP 10 mg (ALLERGY RELIEF) Drug Facts
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
Section 42229-5
Cetirizine Hydrochloride Tablets USP 10 mg (ALLERGY RELIEF)
Drug Facts
Section 50568-5
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.
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.
Warnings
Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.
Directions
| adults and children 6 years and over |
one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. |
| adults 65 years and over |
ask a doctor |
| children under 6 years of age |
ask a doctor |
| consumers with liver or kidney disease |
ask a doctor |
Questions?
call 1-800-206-7821
Manufactured for: Northstar Rx LLC
Memphis, TN 38141
Manufactured by: Aurobindo Pharma Limited
Hyderabad-500 090, India
Code: TS/DRUGS/19/1993
Issued: 05/2024
Other Information
- store between 20° to 25°C (68° to 77°F)
- TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING
Inactive Ingredients
colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide
When Using This Product
- drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
Cetirizine Hydrochloride
Stop Use and Ask A Doctor If
an allergic reaction to this product occurs. Seek medical help right away.
If Pregnant Or Breast Feeding:
- If breast-feeding: not recommended
- if pregnant: ask a health professional before use.
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]
Active Ingredient (in Each Tablet)
Cetirizine hydrochloride USP 10 mg
Structured Label Content
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
Section 42229-5 (42229-5)
Cetirizine Hydrochloride Tablets USP 10 mg (ALLERGY RELIEF)
Drug Facts
Section 50568-5 (50568-5)
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.
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.
Purpose
Antihistamine
Warnings
Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hydroxyzine.
Directions
| adults and children 6 years and over |
one 10 mg tablet once daily; do not take more than one 10 mg tablet in 24 hours. A 5 mg product may be appropriate for less severe symptoms. |
| adults 65 years and over |
ask a doctor |
| children under 6 years of age |
ask a doctor |
| consumers with liver or kidney disease |
ask a doctor |
Questions?
call 1-800-206-7821
Manufactured for: Northstar Rx LLC
Memphis, TN 38141
Manufactured by: Aurobindo Pharma Limited
Hyderabad-500 090, India
Code: TS/DRUGS/19/1993
Issued: 05/2024
How Supplied (HOW SUPPLIED)
Product: 50090-6170
NDC: 50090-6170-0 30 TABLET in a BOTTLE / 48 in a CASE
Other Information (Other information)
- store between 20° to 25°C (68° to 77°F)
- TAMPER EVIDENT: DO NOT USE IF SEAL OVER BOTTLE OPENING IS BROKEN OR MISSING
Inactive Ingredients (Inactive ingredients)
colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide
When Using This Product (When using this product)
- drowsiness may occur
- avoid alcoholic drinks
- alcohol, sedatives, and tranquilizers may increase drowsiness
- be careful when driving a motor vehicle or operating machinery
Cetirizine Hydrochloride
Stop Use and Ask A Doctor If (Stop use and ask a doctor if)
an allergic reaction to this product occurs. Seek medical help right away.
If Pregnant Or Breast Feeding: (If pregnant or breast-feeding:)
- If breast-feeding: not recommended
- if pregnant: ask a health professional before use.
Keep Out of Reach of Children. (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]
Active Ingredient (in Each Tablet) (Active ingredient (in each tablet))
Cetirizine hydrochloride USP 10 mg
Advanced Ingredient Data
Raw Label Data
All Sections (JSON)
Additional Information
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Source: dailymed · Ingested: 2026-02-15T12:03:13.970372 · Updated: 2026-03-14T23:03:12.694901