Theraworx Nerve Relief Foam

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
Theraworx Nerve Relief Foam
Generic name
ONION, HYPERICUM PERFORATUM WHOLE, SANGUINARIA CANADENSIS ROOT
Manufacturer
AVADIM HOLDINGS, INC.
Product type
HUMAN OTC DRUG
SPL set ID
9ed7d5fc-ad84-499b-a774-feedf21ca8d4
SPL ID
fa2348f9-1227-b787-e053-6394a90a4863
Version
3
Effective date
2023-04-25
Source export date
2026-10-12
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/2026-10-12/fa098e7c5cff0b1ab653ce934059d1f4b90b860bafc0383a1f66223ce1037518/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:17:00
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. If eye contact occurs, rinse thoroughly with water. When using this product avoid eye contact store between 32ºF and 120ºF ues only as directed not for ingestion Stop use and ask a doctor if unintended effects occurs. If pregnant or breastfeeding, ask a health professional before use. Keep out of reach of chidlren. If swallowed, get medical help or contact a Poison Control right away.

Reported adverse events (FAERS/openFDA)#

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