Package 69452-449-37

Brand: itch relief

Generic: diphenhydramine hydrochloride and zinc acetate
NDC Package

Package Facts

Identity

Package NDC 69452-449-37
Digits Only 6945244937
Product NDC 69452-449
Description

1 TUBE in 1 CARTON (69452-449-37) / 35.4 g in 1 TUBE

Marketing

Marketing Status
Marketed Since 2024-07-16
Brand itch relief
Generic diphenhydramine hydrochloride and zinc acetate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "178ed513-4f23-8f11-e063-6294a90a109b", "openfda": {"unii": ["TC2D6JAD40", "FM5526K07A"], "rxcui": ["1087026"], "spl_set_id": ["178ed513-4f22-8f11-e063-6294a90a109b"], "manufacturer_name": ["Bionpharma Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 TUBE in 1 CARTON (69452-449-37)  / 35.4 g in 1 TUBE", "package_ndc": "69452-449-37", "marketing_start_date": "20240716"}], "brand_name": "itch relief", "product_id": "69452-449_178ed513-4f23-8f11-e063-6294a90a109b", "dosage_form": "CREAM", "pharm_class": ["Copper Absorption Inhibitor [EPC]", "Decreased Copper Ion Absorption [PE]", "Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "69452-449", "generic_name": "diphenhydramine hydrochloride and zinc acetate", "labeler_name": "Bionpharma Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "itch relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20 mg/g"}, {"name": "ZINC ACETATE", "strength": "1 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20240716", "listing_expiration_date": "20261231"}