FDA.reportPublic FDA data

H- Eczema 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- Eczema Formula
Generic name
ANACARDIUM ORIENTALE, IRIS VERSICOLOR
Manufacturer
Healing Natural Oils
Product type
HUMAN OTC DRUG
SPL set ID
1dca2762-cd9a-4c4c-b2aa-a7dca4b4e414
SPL ID
3628687b-ec01-1a1c-e063-6294a90a8a40
Version
3
Effective date
2025-05-27
Source export date
2026-10-12
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b25dad4aaef9c88f0e827394a34fbbd1ce7d71422fa46b5d1e123befad498c1d/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:46:29
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. If pregnant or breastfeeding consult a doctor before use. 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.