all day allergy

Generic: cetirizine hydrochloride

Labeler: rite aid corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day allergy
Generic Name cetirizine hydrochloride
Labeler rite aid corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Rite Aid Corporation

Identifiers & Regulatory

Product NDC 11822-1002
Product ID 11822-1002_6c4b2dd2-0897-4bcb-a570-6bc6f5332828
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078336
Listing Expiration 2026-12-31
Marketing Start 2021-09-14

Pharmacologic Class

Classes
histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 118221002
Hyphenated Format 11822-1002

Supplemental Identifiers

RxCUI
1014678
UNII
64O047KTOA

Packaging Origin

Original Packager
true

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 (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA078336 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 14 BLISTER PACK in 1 CARTON (11822-1002-1) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (11822-1002-2) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11822-1002-3) / 60 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11822-1002-4) / 120 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11822-1002-7) / 300 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11822-1002-8) / 90 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (6)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6c4b2dd2-0897-4bcb-a570-6bc6f5332828", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["bcbb9f5a-10b6-4a5e-a237-d29693d78103"], "manufacturer_name": ["Rite Aid Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "14 BLISTER PACK in 1 CARTON (11822-1002-1)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "11822-1002-1", "marketing_start_date": "20211207"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1002-2)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-1002-2", "marketing_start_date": "20210914"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1002-3)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-1002-3", "marketing_start_date": "20211207"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1002-4)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-1002-4", "marketing_start_date": "20210914"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1002-7)  / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-1002-7", "marketing_start_date": "20221019"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11822-1002-8)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11822-1002-8", "marketing_start_date": "20220323"}], "brand_name": "all day allergy", "product_id": "11822-1002_6c4b2dd2-0897-4bcb-a570-6bc6f5332828", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11822-1002", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Rite Aid Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "all day allergy", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20210914", "listing_expiration_date": "20261231"}