Package 81522-751-25

Brand: itch relief

Generic: diphenhydramine hcl
NDC Package

Package Facts

Identity

Package NDC 81522-751-25
Digits Only 8152275125
Product NDC 81522-751
Description

74 mL in 1 BOTTLE, SPRAY (81522-751-25)

Marketing

Marketing Status
Marketed Since 2025-08-19
Brand itch relief
Generic diphenhydramine hcl
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "4743491a-42d4-bf24-e063-6294a90a581c", "openfda": {"upc": ["0810025928964"], "unii": ["TC2D6JAD40"], "rxcui": ["1050080"], "spl_set_id": ["47434af6-0fdd-9615-e063-6394a90ab9e8"], "manufacturer_name": ["FSA Store Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "74 mL in 1 BOTTLE, SPRAY (81522-751-25)", "package_ndc": "81522-751-25", "marketing_start_date": "20250819"}], "brand_name": "Itch Relief", "product_id": "81522-751_4743491a-42d4-bf24-e063-6294a90a581c", "dosage_form": "SPRAY", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "81522-751", "generic_name": "Diphenhydramine HCl", "labeler_name": "FSA Store Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20250819", "listing_expiration_date": "20261231"}