OWELL NATURALS Deep Penetrating Pain Relief

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: OWELL NATURALS Deep Penetrating Pain Relief
Generic name: MENTHOL
Manufacturer: OWELL NATURALS BRAND, LLC
Product type: HUMAN OTC DRUG
SPL set ID: b36eb017-ed8d-476e-994b-22b275e00543
SPL ID: 0dba3e8a-1315-7ab3-e063-6394a90a8a6a
Version: 1
Effective date: 2024-01-02
Source export date: 2026-10-27
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a758d73d4d838a965005e6adf01b928e2da86f99be0f8bbaeeb95f3b7acbe418/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 19:56:29

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 17 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		OWELL NATURALS Deep Penetrating Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		OWELL NATURALS BRAND, LLC	openfda.manufacturer_name
ndc	package	83570-443-14	openfda.package_ndc
ndc	package	83570-443-07	openfda.package_ndc
ndc	package	83570-443-02	openfda.package_ndc
ndc	package	83570-443-03	openfda.package_ndc
ndc	product	83570-443	openfda.product_ndc
ndc11	package	83570044303	derived:openfda.package_ndc
ndc11	package	83570044307	derived:openfda.package_ndc
ndc11	package	83570044302	derived:openfda.package_ndc
ndc11	package	83570044314	derived:openfda.package_ndc
rxcui		2672826	openfda.rxcui
spl id		0dba3e8a-1315-7ab3-e063-6394a90a8a6a	id
spl set id		b36eb017-ed8d-476e-994b-22b275e00543	set_id
unii		L7T10EIP3A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For External Use Only. Do Not Use on damaged or broken skin. When using this product keep out of eyes. Rinse with water to remove Do not bandage tightly. Stop use and ask a doctor if rash or irritation develops and lasts. condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help, or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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