equaline all day allergy

Generic: cetirizine hydrochloride

Labeler: united natural foods, inc. dba unfi
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name equaline all day allergy
Generic Name cetirizine hydrochloride
Labeler united natural foods, inc. dba unfi
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
United Natural Foods, Inc. dba UNFI

Identifiers & Regulatory

Product NDC 41163-458
Product ID 41163-458_6e7bab3d-af1a-4b74-921d-99aca2aa0fd3
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA078336
Listing Expiration 2026-12-31
Marketing Start 2008-01-23

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 41163458
Hyphenated Format 41163-458

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 equaline 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
  • 1 BOTTLE in 1 CARTON (41163-458-39) / 30 TABLET, FILM COATED in 1 BOTTLE
  • 14 BLISTER PACK in 1 CARTON (41163-458-66) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 1 BOTTLE in 1 CARTON (41163-458-72) / 60 TABLET, FILM COATED in 1 BOTTLE
source: ndc

Packages (3)

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": "6e7bab3d-af1a-4b74-921d-99aca2aa0fd3", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["491fae66-83b6-4beb-945b-39b9e4e021c5"], "manufacturer_name": ["United Natural Foods, Inc. dba UNFI"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-458-39)  / 30 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-458-39", "marketing_start_date": "20081103"}, {"sample": false, "description": "14 BLISTER PACK in 1 CARTON (41163-458-66)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "41163-458-66", "marketing_start_date": "20080123"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (41163-458-72)  / 60 TABLET, FILM COATED in 1 BOTTLE", "package_ndc": "41163-458-72", "marketing_start_date": "20090909"}], "brand_name": "Equaline all day allergy", "product_id": "41163-458_6e7bab3d-af1a-4b74-921d-99aca2aa0fd3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "41163-458", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "United Natural Foods, Inc. dba UNFI", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Equaline all day allergy", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078336", "marketing_category": "ANDA", "marketing_start_date": "20080123", "listing_expiration_date": "20261231"}