tolnafate
Generic: tolnaftate powder spray
Labeler: topco associates llcDrug Facts
Product Profile
Brand Name
tolnafate
Generic Name
tolnaftate powder spray
Labeler
topco associates llc
Dosage Form
AEROSOL, SPRAY
Routes
Active Ingredients
tolnaftate 1.3 g/130g
Manufacturer
Identifiers & Regulatory
Product NDC
36800-876
Product ID
36800-876_42f45cbf-49ff-8971-e063-6394a90a291d
Product Type
HUMAN OTC DRUG
Marketing Category
OTC MONOGRAPH DRUG
Application Number
M005
Listing Expiration
2026-12-31
Marketing Start
2017-05-22
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36800876
Hyphenated Format
36800-876
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
tolnafate (source: ndc)
Generic Name
tolnaftate powder spray (source: ndc)
Application Number
M005 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1.3 g/130g
Packaging
- 130 g in 1 CAN (36800-876-46)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["TOPICAL"], "spl_id": "42f45cbf-49ff-8971-e063-6394a90a291d", "openfda": {"unii": ["06KB629TKV"], "rxcui": ["705934"], "spl_set_id": ["5f8ae9ab-5e34-7a60-e053-2991aa0a9817"], "manufacturer_name": ["Topco Associates LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "130 g in 1 CAN (36800-876-46)", "package_ndc": "36800-876-46", "marketing_start_date": "20170522"}], "brand_name": "Tolnafate", "product_id": "36800-876_42f45cbf-49ff-8971-e063-6394a90a291d", "dosage_form": "AEROSOL, SPRAY", "product_ndc": "36800-876", "generic_name": "Tolnaftate Powder Spray", "labeler_name": "Topco Associates LLC", "product_type": "HUMAN OTC DRUG", "brand_name_base": "Tolnafate", "active_ingredients": [{"name": "TOLNAFTATE", "strength": "1.3 g/130g"}], "application_number": "M005", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20170522", "listing_expiration_date": "20261231"}