allergy relief-d

Generic: cetirizine hydrochloride and pseudoephedrine hydrochloride

Labeler: cvs pharmacy
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief-d
Generic Name cetirizine hydrochloride and pseudoephedrine hydrochloride
Labeler cvs pharmacy
Dosage Form TABLET, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

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

Manufacturer
CVS PHARMACY

Identifiers & Regulatory

Product NDC 69842-994
Product ID 69842-994_70f4a7eb-7f9e-492b-9b6d-8fb9415f8759
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA090922
Listing Expiration 2026-12-31
Marketing Start 2019-06-30

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 69842994
Hyphenated Format 69842-994

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 allergy relief-d (source: ndc)
Generic Name cetirizine hydrochloride and pseudoephedrine hydrochloride (source: ndc)
Application Number ANDA090922 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
  • 120 mg/1
source: ndc
Packaging
  • 2 BLISTER PACK in 1 CARTON (69842-994-12) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
  • 4 BLISTER PACK in 1 CARTON (69842-994-24) / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (2)

Ingredients (2)

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "70f4a7eb-7f9e-492b-9b6d-8fb9415f8759", "openfda": {"unii": ["64O047KTOA", "6V9V2RYJ8N"], "rxcui": ["1014571"], "spl_set_id": ["54a158e3-f545-4a01-bf8d-e72a286d734c"], "manufacturer_name": ["CVS PHARMACY"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "2 BLISTER PACK in 1 CARTON (69842-994-12)  / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-994-12", "marketing_start_date": "20190630"}, {"sample": false, "description": "4 BLISTER PACK in 1 CARTON (69842-994-24)  / 6 TABLET, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "69842-994-24", "marketing_start_date": "20190630"}], "brand_name": "Allergy Relief-D", "product_id": "69842-994_70f4a7eb-7f9e-492b-9b6d-8fb9415f8759", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]", "alpha-Adrenergic Agonist [EPC]"], "product_ndc": "69842-994", "generic_name": "Cetirizine hydrochloride and pseudoephedrine hydrochloride", "labeler_name": "CVS PHARMACY", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief-D", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "PSEUDOEPHEDRINE HYDROCHLORIDE", "strength": "120 mg/1"}], "application_number": "ANDA090922", "marketing_category": "ANDA", "marketing_start_date": "20190630", "listing_expiration_date": "20261231"}