Package 61010-8300-1

Brand: itch relief

Generic: diphenhydramine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 61010-8300-1
Digits Only 6101083001
Product NDC 61010-8300
Product ID 61010-8300_109674e0-ef83-5844-e063-6394a90ae6b8
Description

.0591 L in 1 BOTTLE, SPRAY (61010-8300-1)

Marketing

Marketing Status
Marketed Since 2013-05-02
Brand itch relief
Generic diphenhydramine hydrochloride
Sample Package No

Linked Drug Pages (1)

Itch Relief ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "109674e0-ef83-5844-e063-6394a90ae6b8", "openfda": {"unii": ["TC2D6JAD40"], "rxcui": ["1050080"], "spl_set_id": ["4f4c801b-d894-4fa3-b024-6ca41a5f2a95"], "manufacturer_name": ["Safetec of America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": ".0591 L in 1 BOTTLE, SPRAY (61010-8300-1)", "package_ndc": "61010-8300-1", "marketing_start_date": "20130502"}], "brand_name": "Itch Relief", "product_id": "61010-8300_109674e0-ef83-5844-e063-6394a90ae6b8", "dosage_form": "LIQUID", "pharm_class": ["Histamine H1 Receptor Antagonists [MoA]", "Histamine-1 Receptor Antagonist [EPC]"], "product_ndc": "61010-8300", "generic_name": "diphenhydramine hydrochloride", "labeler_name": "Safetec of America, Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Itch Relief", "active_ingredients": [{"name": "DIPHENHYDRAMINE HYDROCHLORIDE", "strength": "20.3 g/L"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20130502", "listing_expiration_date": "20261231"}