Package 23667-806-01

Brand: goodsense powder jock itch antifungal

Generic: tolnaftate
NDC Package

Package Facts

Identity

Package NDC 23667-806-01
Digits Only 2366780601
Product NDC 23667-806
Description

130 g in 1 CAN (23667-806-01)

Marketing

Marketing Status
Marketed Since 2017-01-20
Brand goodsense powder jock itch antifungal
Generic tolnaftate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "0b824859-467a-ffcd-e063-6394a90a1e0a", "openfda": {"upc": ["0370030147250"], "unii": ["06KB629TKV"], "rxcui": ["705934"], "spl_set_id": ["46c5fa20-1297-272e-e054-00144ff8d46c"], "manufacturer_name": ["Formulated Solutions, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "130 g in 1 CAN (23667-806-01)", "package_ndc": "23667-806-01", "marketing_start_date": "20170120"}], "brand_name": "GoodSense Powder Jock Itch Antifungal", "product_id": "23667-806_0b824859-467a-ffcd-e063-6394a90a1e0a", "dosage_form": "SPRAY", "product_ndc": "23667-806", "generic_name": "TOLNAFTATE", "labeler_name": "Formulated Solutions, LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "GoodSense Powder Jock Itch Antifungal", "active_ingredients": [{"name": "TOLNAFTATE", "strength": "10 mg/g"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170120", "listing_expiration_date": "20261231"}