allergy relief

Generic: cetirizine hydrochloride

Labeler: h e b
NDC Directory HUMAN OTC DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name allergy relief
Generic Name cetirizine hydrochloride
Labeler h e b
Dosage Form SOLUTION
Routes
ORAL
Active Ingredients

cetirizine hydrochloride 1 mg/mL

Manufacturer
H E B

Identifiers & Regulatory

Product NDC 37808-106
Product ID 37808-106_3e05caf8-84cf-478f-9401-762f51c9e796
Product Type HUMAN OTC DRUG
Marketing Category ANDA
Application Number ANDA201546
Listing Expiration 2026-12-31
Marketing Start 2011-05-20

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 37808106
Hyphenated Format 37808-106

Supplemental Identifiers

RxCUI
1014673
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 ANDA201546 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 CARTON (37808-106-08) / 120 mL in 1 BOTTLE
source: ndc

Packages (1)

Ingredients (1)

cetirizine hydrochloride (1 mg/mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3e05caf8-84cf-478f-9401-762f51c9e796", "openfda": {"unii": ["64O047KTOA"], "rxcui": ["1014673"], "spl_set_id": ["fdd3f9a0-b4be-498a-b8e0-1a9740399736"], "manufacturer_name": ["H E B"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (37808-106-08)  / 120 mL in 1 BOTTLE", "package_ndc": "37808-106-08", "marketing_start_date": "20180412"}], "brand_name": "Allergy Relief", "product_id": "37808-106_3e05caf8-84cf-478f-9401-762f51c9e796", "dosage_form": "SOLUTION", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "37808-106", "generic_name": "Cetirizine Hydrochloride", "labeler_name": "H E B", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Allergy Relief", "active_ingredients": [{"name": "CETIRIZINE HYDROCHLORIDE", "strength": "1 mg/mL"}], "application_number": "ANDA201546", "marketing_category": "ANDA", "marketing_start_date": "20110520", "listing_expiration_date": "20261231"}