foot odor control powder

Generic: tolnaftate

Labeler: premier brands of america inc.
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name foot odor control powder
Generic Name tolnaftate
Labeler premier brands of america inc.
Dosage Form AEROSOL, SPRAY
Routes
TOPICAL
Active Ingredients

tolnaftate 1.3 g/113g

Manufacturer
Premier Brands of America Inc.

Identifiers & Regulatory

Product NDC 56104-252
Product ID 56104-252_45c7c11b-d629-aee8-e063-6294a90a401d
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M005
Listing Expiration 2026-12-31
Marketing Start 2021-09-29

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 56104252
Hyphenated Format 56104-252

Supplemental Identifiers

UNII
06KB629TKV

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name foot odor control powder (source: ndc)
Generic Name tolnaftate (source: ndc)
Application Number M005 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 1.3 g/113g
source: ndc
Packaging
  • 113 g in 1 CAN (56104-252-01)
source: ndc

Packages (1)

56104-252-01 113 g in 1 CAN (56104-252-01)

Ingredients (1)

tolnaftate (1.3 g/113g)

Linked Drug Pages (1)

Foot Odor Control Powder ndc-match (0.9)

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"}