Hempvana Ultra Strength Pain Relief - Overnight

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 Ultra Strength Pain Relief - Overnight
Generic name
LIDOCAINE
Manufacturer
Telebrands Corp
Product type
HUMAN OTC DRUG
SPL set ID
1030d478-6805-6579-e063-6294a90a0c76
SPL ID
284c9a8c-9556-070a-e063-6394a90aec2a
Version
3
Effective date
2024-12-02
Source export date
2026-10-30
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/2026-10-30/a3e33fe073aa0aa94eb690c6684c74434c63cebfbf7c5530205a2c3e957ecb8b/drug-label-0012-of-0014.json.zip
Source manifest SHA-256
b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
Import run
20261102T182004Z
Imported at
2026-11-02 19:47:16
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. ■ do not use in large quantities, particularly over raw surfaces or blistered areas. 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.