Package 42961-218-01

Brand: xpect extra strength itch relief

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 42961-218-01
Digits Only 4296121801
Product NDC 42961-218
Description

59.1 mL in 1 BOTTLE, SPRAY (42961-218-01)

Marketing

Marketing Status
Marketed Since 2022-05-16
Brand xpect extra strength itch relief
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "43b08582-e9bb-4ba4-a2ca-7eab3c9c16c6", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1050080"], "spl_set_id": ["a373b2c3-5c58-4b64-9358-bdf42dfce08c"], "manufacturer_name": ["Cintas Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "59.1 mL in 1 BOTTLE, SPRAY (42961-218-01)", "package_ndc": "42961-218-01", "marketing_start_date": "20220516"}], "brand_name": "Xpect Extra Strength Itch Relief", "product_id": "42961-218_43b08582-e9bb-4ba4-a2ca-7eab3c9c16c6", "dosage_form": "SPRAY", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "42961-218", "generic_name": "Diphenhydramine Hydrochloride", "labeler_name": "Cintas Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Xpect Extra Strength Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "2 mg/100mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20220516", "listing_expiration_date": "20261231"}