Label: ALL DAY ALLERGY RELIEF 24 HOUR- cetirizine hydrochloride tablet
- NDC Code(s): 70253-129-30
- Packager: OUR FAMILY (NASH FINCH COMPANY)
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
NOTE: Most over the counter (OTC) are not reviewed and approved by the FDA. However, they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.
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- Active ingredient (in each tablet)
Cetirizine HCl 10 mgClose
temporarily relieves these symptoms due to hay fever or other upper respiratory allergies:
- runny nose
- 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.
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
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.
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)
- Inactive ingredients
lactose monohydrate, magnesium stearate, polyethylene glycol, polyvinyl alcohol, povidone, starch, talc, and titanium dioxideClose
- Questions or comments?
Call 1-877-753-3935 Monday-Friday 9AM-5PM ESTClose
- Principal Display Panel
Original Prescription Strength
Allergy Relief of: Runny Nose, Sneezing, Itchy, Watery Eyes, Itchy Throat or Nose
Compare to the Active Ingredient in Zyrtec®*
ALL DAY ALLERGY
CETIRIZINE HYDROCHLORIDE TABLETS, 10 MG
INDOOR & OUTDOOR ALLERGIES
*This product is not manufactured or distributed by McNeil Consumer Healthcare, Division of McNeil-PPC, Inc., owner of the registered trademark Zyrtec®.
NASH FINCH COMPANY ©2004, 1996
7600 FRANCE AVE S, MPLS, MN 55435
THIS PRODUCT IS PACKAGED IN A CHILD RESISTANT AND TAMPER EVIDENT PACKAGE. USE ONLY IF BLISTERS ARE INTACT.
KEEP OUTER CARTON FOR COMPLETE WARNINGS AND PRODUCT INFORMATIONClose
- Product Label
Our Family All Day Allergy Tablets
- INGREDIENTS AND APPEARANCE
ALL DAY ALLERGY RELIEF 24 HOUR
cetirizine hcl tablet
Product Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:70253-129 Route of Administration ORAL DEA Schedule Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE - UNII:YO7261ME24) CETIRIZINE HYDROCHLORIDE 10 mg Inactive Ingredients Ingredient Name Strength LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X) MAGNESIUM STEARATE (UNII: 70097M6I30) POLYETHYLENE GLYCOLS (UNII: 3WJQ0SDW1A) POVIDONES (UNII: FZ989GH94E) STARCH, CORN (UNII: O8232NY3SJ) TALC (UNII: 7SEV7J4R1U) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) POLYVINYL ALCOHOL (UNII: 532B59J990) Product Characteristics Color WHITE Score no score Shape ROUND Size 8mm Flavor Imprint Code IP46 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:70253-129-30 2 in 1 CARTON 1 15 in 1 BLISTER PACK Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA078780 03/15/2013 Labeler - OUR FAMILY (NASH FINCH COMPANY) (006962294) Registrant - P and L Development of New York Corporation (800014821)