Label: DG HEALTH ALL DAY ALLERGY- cetirizine hydrochloride capsule, liquid filled
- NDC Code(s): 55910-710-49, 55910-710-63
- Packager: Dolgencorp, LLC
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated June 1, 2021
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- Official Label (Printer Friendly)
- Active ingredient (in each capsule)
- Purpose
- Uses
-
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.
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
- Keep out of reach of children.
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Directions
adults and children 6 years and over
one 10 mg capsule once daily; do not take more than one 10 mg capsule 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
- Inactive ingredients
- Questions or comments?
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Package/Label Principal Display Panel
Compare to the active ingredient of Zyrtec® Liquid Gels
Original Prescription Strength
All Day Allergy
Cetirizine Hydrochloride Capsules, 10 mg
Antihistamine
Indoor & Outdoor Allergies
24 Hour Relief of: ● Sneezing ● Runny nose ● Itchy, watery eyes ● Itchy throat or nose
24 HOUR
Actual Liquid Gel Size
40 Liquid Gels*
*Liquid-Filled Capsules
10 mg
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INGREDIENTS AND APPEARANCE
DG HEALTH ALL DAY ALLERGY
cetirizine hydrochloride capsule, liquid filledProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:55910-710 Route of Administration ORAL 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 BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) GELATIN, UNSPECIFIED (UNII: 2G86QN327L) GLYCERIN (UNII: PDC6A3C0OX) MANNITOL (UNII: 3OWL53L36A) POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ) WATER (UNII: 059QF0KO0R) SODIUM HYDROXIDE (UNII: 55X04QC32I) SORBITAN (UNII: 6O92ICV9RU) SORBITOL (UNII: 506T60A25R) Product Characteristics Color YELLOW Score no score Shape OVAL Size 13mm Flavor Imprint Code 10 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:55910-710-63 1 in 1 CARTON 05/26/2021 1 25 in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:55910-710-49 1 in 1 CARTON 05/26/2021 2 40 in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA207235 05/26/2021 Labeler - Dolgencorp, LLC (068331990)