Alleroff
FDA Label NDC 16853-1305
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Corporacion Infarmasa for the product Alleroff (NDC 16853-1305). 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 otc - active ingredient, otc - ask doctor, otc - ask doctor/pharmacist, otc - do not use, otc - keep out of reach of children, otc - pregnancy or breast feeding, otc - stop use, otc - purpose, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Ask Doctor
Otc - Ask Doctor/Pharmacist
Ask a doctor or pharmacist before use if you are taking tranquilizers or sedatives.
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
Otc - Do Not Use
Do not use if you have ever had an allergic reaction to this product or any of its ingredients or to an antihistamine containing hidroxyzine
Otc - 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)
Otc - Pregnancy Or Breast Feeding
If pregnant or breast feeding:
- if breast feeding: not recommended
- if pregnant: ask a health professional before use
Otc - Stop Use
Stop use and ask a doctor if an allergic reaction to this product occurs. Seek medical help right away.
Otc - Purpose
Uses
Temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- Runny Nose
- Itchy,water eyes
- Itching of the nose or throat
- Sneezing
Otc - Questions
If you have questions of a medical nature, please contact your pharmacist, doctor or health care profesional
Questions or comments? 561 338 5221
Storage And Handling
Do not use if blister unit is broken or lorn
Store between 20°C to 25°C ( 68°F to 77°F)
Dosage & Administration
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 strenght may be appropiate for less severe symptoms
Adults 65 years and over Ask a Doctor
Children under 6 years of age Ask a Doctor
Consumer with liver or kidney disease Ask a Doctor
Inactive Ingredient
Microcrystalline Cellulose, Lactose Monohydrate, Crosscaramellose Sodium, Magnesium Stearate
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