Natures Willow Balm Roll On 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: Natures Willow Balm Roll On Pain Relief
Generic name: MENTHOL
Manufacturer: WB Ventures LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3b1834e6-75cd-5380-e063-6294a90ad1d5
SPL ID: 561e3122-1c29-f776-e063-6394a90a5a74
Version: 2
Effective date: 2026-07-08
Source export date: 2026-10-12
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/acb9b4700b9af1bdda1c389c7b35bfe38fd6d1a62aa48d17832812be4029b84f/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 03:12:37

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 · 11 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Natures Willow Balm Roll On Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		WB Ventures LLC	openfda.manufacturer_name
ndc	package	73498-029-01	openfda.package_ndc
ndc	product	73498-029	openfda.product_ndc
ndc11	package	73498002901	derived:openfda.package_ndc
rxcui		1798269	openfda.rxcui
spl id		561e3122-1c29-f776-e063-6394a90a5a74	id
spl set id		3b1834e6-75cd-5380-e063-6294a90ad1d5	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 wounds or damaged skin When using this product avoid contact with eyes do not bandage tightly Stop use and ask a doctor if conditions worsen symptoms persist for more than 7 days or clear up and occur again within a few days 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.