Package 11509-5058-1

Brand: vagisil anti-itch medicated wipes maximum strength

Generic: pramoxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 11509-5058-1
Digits Only 1150950581
Product NDC 11509-5058
Description

20 PACKET in 1 POUCH (11509-5058-1) / 3.4 g in 1 PACKET

Marketing

Marketing Status
Marketed Since 2005-06-28
Brand vagisil anti-itch medicated wipes maximum strength
Generic pramoxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "d52bff6a-9386-4ff7-a2ff-bef4a6ad07f8", "openfda": {"unii": ["88AYB867L5"], "rxcui": ["1039541", "1039550"], "spl_set_id": ["b848f53d-8aea-4efe-aa2c-009d5121fc33"], "manufacturer_name": ["Combe Incorporated"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 PACKET in 1 POUCH (11509-5058-1)  / 3.4 g in 1 PACKET", "package_ndc": "11509-5058-1", "marketing_start_date": "20050628"}], "brand_name": "VAGISIL Anti-Itch Medicated Wipes Maximum Strength", "product_id": "11509-5058_d52bff6a-9386-4ff7-a2ff-bef4a6ad07f8", "dosage_form": "CLOTH", "product_ndc": "11509-5058", "generic_name": "pramoxine hydrochloride", "labeler_name": "Combe Incorporated", "product_type": "HUMAN OTC DRUG", "brand_name_base": "VAGISIL Anti-Itch Medicated Wipes Maximum Strength", "active_ingredients": [{"name": "PRAMOXINE HYDROCHLORIDE", "strength": "10 mg/g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20050628", "listing_expiration_date": "20261231"}