H-Athletes Foot Formula

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
H-Athletes Foot Formula
Generic name
CALENDULA OFFICINALIS, LYCOPODIUM CLAVATUM, THUJA OCCIDENTALIS
Manufacturer
Healing Natural Oils LLC
Product type
HUMAN OTC DRUG
SPL set ID
26087810-80ad-471e-8ab8-53d84dc7a792
SPL ID
0fd474ab-5177-438d-bcb5-30dad4090ae0
Version
2
Effective date
2017-12-27
Source export date
2026-11-06
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/7dfa569f2d8f065241260fd9a4886d0ef0a3120fd6ee31d6d07c234e689e8c91/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run
20261106T075659Z
Imported at
2026-11-06 08:18:00
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 · 3 matching rows.

warnings

Warnings: For external use only. Perform skin test prior to initial use. Do not use if pregnant or breastfeeding. Keep out of reach of children. Keep away from eyes and mucous membranes. If swallowed get medical help or contact a Poison Control Center right away. Discontinue use if irritation occurs. Consult a doctor if symptoms worsen after 7 days.

warnings table

<table ID="ic728d8da-35c2-4475-833b-9b060849cdb4" width="100%"> <tbody> <tr> <td> <paragraph> <content styleCode="bold"> For external use only.</content> </paragraph>Perform skin test prior to initial use.</td> </tr> </tbody> </table>

warnings table

<table width="100%" ID="ic83e7d26-9c52-4c96-87c2-60039f6d5ee3"> <tbody> <tr> <td>Discontinue use if irritation occurs.</td> </tr> </tbody> </table>

Reported adverse events (FAERS/openFDA)#

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