H-Varicose Veins 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-Varicose Veins Formula
Generic name
AESCULUS HIPPOCASTANUM, COLLINSONIA CANADENSIS
Manufacturer
Healing Natural Oils LLC
Product type
HUMAN OTC DRUG
SPL set ID
a54bbdaf-8dcc-4a5d-8ea3-ffc47abfba3f
SPL ID
509dc689-58a9-cd6f-e063-6394a90a007f
Version
6
Effective date
2026-04-29
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:18:11
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.