Frankincense and Myrrh Neuropathy

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
Frankincense and Myrrh Neuropathy
Generic name
ACONITUM NAPELLUS, BRYONIA ALBA, HYPERICUM PERFORATUM
Manufacturer
Wise Consumer Products
Product type
HUMAN OTC DRUG
SPL set ID
9310c00d-c60a-4e9a-b1c1-06e6bdbb24ef
SPL ID
d246535b-bbe5-06a0-e053-2a95a90a9248
Version
4
Effective date
2021-12-03
Source export date
2026-09-28
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e78bf8aa9f90ab13e640d254dfbd4fe5bfeca4995ec5f9d51bce3356e249cab7/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:33:55
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. Do not apply to wounds, broken or damaged skin apply over large areas of the body When using this product avoid contact with eyes, mouth, nose or mucous membranes do not bandage tightly Stop use and ask a doctor if you are experiencing nerve pain in the feet and hands that includes burning, shooting, prickling/tingling pains, numbness or itching as these can be signs of diabetic neuropathy. See a healthcare professional regularly if you have or suspect you have these symptoms. condition worsens if symptoms persist for more than 7 days or clear up and occur again within a few days excessive skin irritation occurs If pregnant or breastfeeding , ask a health care professional before use. Keep out of reach of children. 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.