Package 0225-0495-33

Brand: itch x

Generic: benzyl alcohol/pramoxine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0225-0495-33
Digits Only 0225049533
Product NDC 0225-0495
Description

35.4 g in 1 TUBE (0225-0495-33)

Marketing

Marketing Status
Marketed Since 2014-09-19
Brand itch x
Generic benzyl alcohol/pramoxine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "2888be26-0ebc-ab78-e063-6394a90ada63", "openfda": {"nui": ["N0000181811"], "unii": ["LKG8494WBH", "88AYB867L5"], "rxcui": ["1293632", "1293634"], "spl_set_id": ["03c16d33-8f59-0184-e054-00144ff8d46c"], "pharm_class_epc": ["Pediculicide [EPC]"], "manufacturer_name": ["BF ASCHER AND CO INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "35.4 g in 1 TUBE (0225-0495-33)", "package_ndc": "0225-0495-33", "marketing_start_date": "20140919"}], "brand_name": "ITCH X", "product_id": "0225-0495_2888be26-0ebc-ab78-e063-6394a90ada63", "dosage_form": "GEL", "pharm_class": ["Pediculicide [EPC]"], "product_ndc": "0225-0495", "generic_name": "BENZYL ALCOHOL/PRAMOXINE HYDROCHLORIDE", "labeler_name": "BF ASCHER AND CO INC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "ITCH X", "active_ingredients": [{"name": "BENZYL ALCOHOL", "strength": "10 g/100g"}, {"name": "PRAMOXINE HYDROCHLORIDE", "strength": "1 g/100g"}], "application_number": "M017", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20140919", "listing_expiration_date": "20261231"}