Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate

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
Hempvana Maximum Strength Pain Relief Cream 10% Trolamine Salicylate
Generic name
TROLAMINE SALICYLATE
Manufacturer
TELEBRANDS CORP
Product type
HUMAN OTC DRUG
SPL set ID
2d685602-5cd6-3b36-e063-6394a90a3c5d
SPL ID
2d686088-00da-d0d1-e063-6294a90acf89
Version
1
Effective date
2025-02-05
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:53:56
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only Allergy alert: If prone to allergic reaction from aspirin or salicylates, consult a doctor before use. When using this product Use only as directed. Read and follow all directions and warnings on this label. Do not bandage tightly or apply local heat (such as heating pads) to the area of use. Avoid contact with eyes or mucous membranes. Do not apply to wounds or damaged, broken, or irritated skin. Do not use at the same time as other topical analgesics. Stop use and ask a doctor if Condition worsens Symptoms persist for more than 7 days or clear up and occur again within a few days Redness is present or irritation develops If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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