Package 56104-252-01
Brand: foot odor control powder
Generic: tolnaftatePackage Facts
Identity
Package NDC
56104-252-01
Digits Only
5610425201
Product NDC
56104-252
Description
113 g in 1 CAN (56104-252-01)
Marketing
Marketing Status
Brand
foot odor control powder
Generic
tolnaftate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "45c7c11b-d629-aee8-e063-6294a90a401d", "openfda": {"unii": ["06KB629TKV"], "spl_set_id": ["edb0a2da-aaa1-3b9b-e053-2995a90a5012"], "manufacturer_name": ["Premier Brands of America Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "113 g in 1 CAN (56104-252-01)", "package_ndc": "56104-252-01", "marketing_start_date": "20210929"}], "brand_name": "Foot Odor Control Powder", "product_id": "56104-252_45c7c11b-d629-aee8-e063-6294a90a401d", "dosage_form": "AEROSOL, SPRAY", "product_ndc": "56104-252", "generic_name": "Tolnaftate", "labeler_name": "Premier Brands of America Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Foot Odor Control Powder", "active_ingredients": [{"name": "TOLNAFTATE", "strength": "1.3 g/113g"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20210929", "listing_expiration_date": "20261231"}