fungifoam

Generic: tolnaftate

Labeler: the tetra corporation
NDC Directory HUMAN OTC DRUG OTC MONOGRAPH DRUG Inactive Finished

Drug Facts

Product Profile

Brand Name fungifoam
Generic Name tolnaftate
Labeler the tetra corporation
Dosage Form AEROSOL, FOAM
Routes
TOPICAL
Active Ingredients

tolnaftate 10 mg/mL

Manufacturer
The Tetra Corporation

Identifiers & Regulatory

Product NDC 49406-004
Product ID 49406-004_4c5c1f4d-1131-c3d0-e063-6394a90a88e2
Product Type HUMAN OTC DRUG
Marketing Category OTC MONOGRAPH DRUG
Application Number M005
Listing Expiration 2027-12-31
Marketing Start 2020-07-13

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 49406004
Hyphenated Format 49406-004

Supplemental Identifiers

RxCUI
1356533 1356538
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 fungifoam (source: ndc)
Generic Name tolnaftate (source: ndc)
Application Number M005 (source: ndc)
Routes
TOPICAL
source: ndc

Resolved Composition

Strengths
  • 10 mg/mL
source: ndc
Packaging
  • 1 BOTTLE in 1 BOX (49406-004-75) / 75 mL in 1 BOTTLE
source: ndc

Packages (1)

49406-004-75 1 BOTTLE in 1 BOX (49406-004-75) / 75 mL in 1 BOTTLE

Ingredients (1)

tolnaftate (10 mg/mL)

Linked Drug Pages (1)

FungiFoam ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["TOPICAL"], "spl_id": "4c5c1f4d-1131-c3d0-e063-6394a90a88e2", "openfda": {"unii": ["06KB629TKV"], "rxcui": ["1356533", "1356538"], "spl_set_id": ["2449e8e5-9d7e-4119-9e7a-378efe55f875"], "manufacturer_name": ["The Tetra Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 BOX (49406-004-75)  / 75 mL in 1 BOTTLE", "package_ndc": "49406-004-75", "marketing_start_date": "20200713"}], "brand_name": "FungiFoam", "product_id": "49406-004_4c5c1f4d-1131-c3d0-e063-6394a90a88e2", "dosage_form": "AEROSOL, FOAM", "product_ndc": "49406-004", "generic_name": "TOLNAFTATE", "labeler_name": "The Tetra Corporation", "product_type": "HUMAN OTC DRUG", "brand_name_base": "FungiFoam", "active_ingredients": [{"name": "TOLNAFTATE", "strength": "10 mg/mL"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20200713", "listing_expiration_date": "20271231"}