allergy relief

Generic: cetirizine hydrochloride

Labeler: magno-humphries, inc.
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name cetirizine hydrochloride
Labeler magno-humphries, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 10 mg/1

Manufacturer
Magno-Humphries, Inc.

Identifiers & Regulatory

Product NDC 54257-270
Product ID 54257-270_cf6d242a-ce61-23b7-e053-2a95a90a856c
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA209274
Listing Expiration 2026-12-31
Marketing Start 2020-01-24

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 54257270
Hyphenated Format 54257-270

Supplemental Identifiers

RxCUI
1014678
UPC
0043292564997 0043292565277
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 allergy relief (source: ndc)
Generic Name cetirizine hydrochloride (source: ndc)
Application Number ANDA209274 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (54257-270-02)
  • 500 TABLET in 1 BOTTLE (54257-270-05)
source: ndc

Packages (2)

54257-270-02 100 TABLET in 1 BOTTLE (54257-270-02) 54257-270-05 500 TABLET in 1 BOTTLE (54257-270-05)

Ingredients (1)

cetirizine hydrochloride (10 mg/1)

Linked Drug Pages (1)

Allergy Relief ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "cf6d242a-ce61-23b7-e053-2a95a90a856c", "openfda": {"upc": ["0043292564997", "0043292565277"], "unii": ["64O047KTOA"], "rxcui": ["1014678"], "spl_set_id": ["f0a3e654-5fec-4f98-84da-4c30500633b4"], "manufacturer_name": ["Magno-Humphries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (54257-270-02)", "package_ndc": "54257-270-02", "marketing_start_date": "20200124"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (54257-270-05)", "package_ndc": "54257-270-05", "marketing_start_date": "20200124"}], "brand_name": "Allergy Relief", "product_id": "54257-270_cf6d242a-ce61-23b7-e053-2a95a90a856c", "dosage_form": "TABLET", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "54257-270", "generic_name": "CETIRIZINE HYDROCHLORIDE", "labeler_name": "Magno-Humphries, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209274", "marketing_category": "ANDA", "marketing_start_date": "20200124", "listing_expiration_date": "20261231"}