all day allergy relief
Generic: cetirizine hydrochloride
Labeler: dolgencorp, inc.Drug Facts
Product Profile
Brand Name
all day allergy relief
Generic Name
cetirizine hydrochloride
Labeler
dolgencorp, inc.
Dosage Form
TABLET
Routes
Active Ingredients
cetirizine hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
55910-269
Product ID
55910-269_0c774d83-58dd-d9b3-e063-6394a90a6f7a
Product Type
HUMAN OTC DRUG
Marketing Category
ANDA
Application Number
ANDA078933
Listing Expiration
2026-12-31
Marketing Start
2023-12-20
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55910269
Hyphenated Format
55910-269
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
all day allergy relief (source: ndc)
Generic Name
cetirizine hydrochloride (source: ndc)
Application Number
ANDA078933 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 1 BOTTLE in 1 CARTON (55910-269-58) / 45 TABLET in 1 BOTTLE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0c774d83-58dd-d9b3-e063-6394a90a6f7a", "openfda": {"upc": ["0355910269581"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["0643ea78-9709-8526-e063-6394a90a227b"], "manufacturer_name": ["DOLGENCORP, INC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (55910-269-58) / 45 TABLET in 1 BOTTLE", "package_ndc": "55910-269-58", "marketing_start_date": "20231220"}], "brand_name": "All Day Allergy Relief", "product_id": "55910-269_0c774d83-58dd-d9b3-e063-6394a90a6f7a", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "55910-269", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "DOLGENCORP, INC.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "All Day Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078933", "marketing_category": "ANDA", "marketing_start_date": "20231220", "listing_expiration_date": "20261231"}