all day allergy d

Generic: cetirizine hydrochloride, pseudoephedrine hydrochloride

Labeler: kroger company
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name all day allergy d
Generic Name cetirizine hydrochloride, pseudoephedrine hydrochloride
Labeler kroger company
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 5 mg/1, pseudoephedrine hydrochloride 120 mg/1

Manufacturer
Kroger Company

Identifiers & Regulatory

Product NDC 30142-450
Product ID 30142-450_ae0a349c-4ee1-42c2-bef0-b85e1de31e24
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA210719
Listing Expiration 2026-12-31
Marketing Start 2020-04-02

Pharmacologic Class

Classes
adrenergic alpha-agonists [moa] histamine h1 receptor antagonists [moa] histamine-1 receptor antagonist [epc] alpha-adrenergic agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 30142450
Hyphenated Format 30142-450

Supplemental Identifiers

RxCUI
1014571
UNII
64O047KTOA 6V9V2RYJ8N

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 d (source: ndc)
Generic Name cetirizine hydrochloride, pseudoephedrine hydrochloride (source: ndc)
Application Number ANDA210719 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 24 BLISTER PACK in 1 CARTON (30142-450-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

30142-450-62 24 BLISTER PACK in 1 CARTON (30142-450-62) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Ingredients (2)

cetirizine hydrochloride (5 mg/1) pseudoephedrine hydrochloride (120 mg/1)

Linked Drug Pages (1)

all day allergy d ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "ae0a349c-4ee1-42c2-bef0-b85e1de31e24", "openfda": {"unii": ["64O047KTOA", "6V9V2RYJ8N"], "rxcui": ["1014571"], "spl_set_id": ["2f1df816-311b-444a-8040-21227016614b"], "manufacturer_name": ["Kroger Company"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "24 BLISTER PACK in 1 CARTON (30142-450-62)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "30142-450-62", "marketing_start_date": "20200402"}], "brand_name": "all day allergy d", "product_id": "30142-450_ae0a349c-4ee1-42c2-bef0-b85e1de31e24", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "30142-450", "generic_name": "cetirizine hydrochloride, pseudoephedrine hydrochloride", "labeler_name": "Kroger Company", "product_type": "HUMAN OTC DRUG", "brand_name_base": "all day allergy d", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA210719", "marketing_category": "ANDA", "marketing_start_date": "20200402", "listing_expiration_date": "20261231"}