Active Ingredient (In Each Tablet)
Cetirizine HCl 10 mg
Allergy Relief Tablet
FDA Label NDC 71335-9733
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Bryant Ranch Prepack for the product Allergy Relief (NDC 71335-9733). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient (in each tablet), purpose, uses, do not use, ask a doctor before use if you have, ask a doctor or pharmacist before use if you are, when using this product, stop use and ask a doctor if, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Antihistamine
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
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.
Ask A Doctor Before Use If You Have
liver or kidney disease. Your doctor should determine if you need a different dose.
Ask A Doctor Or Pharmacist Before Use If You Are
taking tranquilizers or sedatives.
When Using This Product
- drowsiness may occur
- alcohol, sedatives, and tranquilizers may increase drowsiness
- avoid alcoholic drinks
- be careful when driving a motor vehicle or operating machinery
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 (1-800-222-1222) right away.
Directions
| adults and children 6 years and over | Take 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 |
Other Information
- store between 20° to 25°C (68° to 77°F)
- contains no ingredient made from a gluten-containing grain(wheat, barley or rye)
Inactive Ingredients
colloidal silicon dioxide, croscarmellose sodium, hypromellose, lactose monohydrate, magnesium stearate, microcrystalline cellulose, polyethylene glycol, titanium dioxide
Questions Or Comments?
Call 1-888-588-1418 Monday-Friday 9AM-5PM EST
Principal Display Panel
*Compare to the active ingredient in Zyrtec®
Allergy Relief
Cetirizine HCl Tablets USP, 10 mg/Antihistamine
Indoor & Outdoor Allergies
24 hour relief of
- Sneezing
- Runny Nose
- Itchy, Watery Eyes
- Itchy Throat or Nose
Original Prescription Strength
Tablets
*This product is not manufactured or distributed by McNeil Consumer Healthcare, distributor of Zyrtec®.
TAMPER EVIDENT: DO NOT USE IF PRINTED SAFETY SEAL UNDER CAP IS BROKEN OR MISSING.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATION.
Distributed by:
Camber Consumer Care Inc, Piscataway, NJ 08854, USA
How Supplied
NDC: 71335-9733-1: 30 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-2: 14 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-3: 7 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-4: 10 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-5: 15 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-6: 90 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-7: 20 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-8: 60 Tablets in a BOTTLE, PLASTIC
NDC: 71335-9733-9: 100 Tablets in a BOTTLE, PLASTIC
Package Label.Principal Display Panel
Cetirizine Hydrochloride 10 mg Tablet
Label (Lbl713359733)
* Please review the disclaimer below.
