CR-371059 Tolnaftate 1%

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name
CR-371059 Tolnaftate 1%
Generic name
CR-371059 TOLNAFTATE 1%
Manufacturer
A-S Medication Solutions
Product type
HUMAN OTC DRUG
SPL set ID
bb4e4612-850c-4863-954d-7ad0500b9c05
SPL ID
1604ba71-7e8b-4596-8dd0-5488981cc96c
Version
5
Effective date
2023-11-01
Source export date
2026-10-12
Source partition
12
Source file
https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:51:55
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings • For External Use Only • This product is not effective on the scalp or nails When using this product Avoid contact with the eyes Stop use and ask a doctor if • Irritation occurs • There is no improvement within 4 weeks Keep out of reach of children • If swallowed, get medical help or contact a Poisen Control Center (1-800-222-1222) right away • Do not use on children under 2 years of age except under the advice and supervision of a doctor

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.