up and up allergy relief

Generic: cetirizine hydrochloride

Labeler: target corporation
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name up and up allergy relief
Generic Name cetirizine hydrochloride
Labeler target corporation
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Target Corporation

Identifiers & Regulatory

Product NDC 11673-502
Product ID 11673-502_8f32f92c-9043-439d-a318-8f4ae6b1ad39
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078336
Listing Expiration 2026-12-31
Marketing Start 2014-12-17

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 11673502
Hyphenated Format 11673-502

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 up and up allergy relief (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
  • 1 BOTTLE in 1 CARTON (11673-502-00) / 90 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-502-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 2 BOTTLE in 1 CARTON (11673-502-48) / 90 TABLET, FILM COATED in 1 BOTTLE (11673-502-75)
  • 1 BOTTLE in 1 CARTON (11673-502-72) / 60 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-502-76) / 120 TABLET, FILM COATED in 1 BOTTLE
  • 1 BOTTLE in 1 CARTON (11673-502-87) / 300 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (6)

11673-502-00 1 BOTTLE in 1 CARTON (11673-502-00) / 90 TABLET, FILM COATED in 1 BOTTLE 11673-502-39 1 BOTTLE in 1 CARTON (11673-502-39) / 30 TABLET, FILM COATED in 1 BOTTLE 11673-502-48 2 BOTTLE in 1 CARTON (11673-502-48) / 90 TABLET, FILM COATED in 1 BOTTLE (11673-502-75) 11673-502-72 1 BOTTLE in 1 CARTON (11673-502-72) / 60 TABLET, FILM COATED in 1 BOTTLE 11673-502-76 1 BOTTLE in 1 CARTON (11673-502-76) / 120 TABLET, FILM COATED in 1 BOTTLE 11673-502-87 1 BOTTLE in 1 CARTON (11673-502-87) / 300 TABLET, FILM COATED in 1 BOTTLE

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Up and Up Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8f32f92c-9043-439d-a318-8f4ae6b1ad39", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["ce93ca5b-2a65-4873-9686-926c44076c6c"], "manufacturer_name": ["Target Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-502-00)  / 90 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-502-00", "marketing_start_date": "20150311"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-502-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-502-39", "marketing_start_date": "20141217"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (11673-502-48)  / 90 TABLET, FILM COATED in 1 BOTTLE (11673-502-75)", "package_ndc": "11673-502-48", "marketing_start_date": "20141217"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-502-72)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-502-72", "marketing_start_date": "20210106"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-502-76)  / 120 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-502-76", "marketing_start_date": "20191018"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (11673-502-87)  / 300 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "11673-502-87", "marketing_start_date": "20160314"}], "brand_name": "Up and Up Allergy Relief", "product_id": "11673-502_8f32f92c-9043-439d-a318-8f4ae6b1ad39", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "11673-502", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "Target Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Up and Up Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20141217", "listing_expiration_date": "20261231"}