Pain Be Gone

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: Pain Be Gone
Generic name: MENTHOL
Manufacturer: Back to Earth Inc.
Product type: HUMAN OTC DRUG
SPL set ID: f49e718b-ef89-b648-e053-2a95a90a96c8
SPL ID: 2ce15484-38f2-014d-e063-6294a90aced2
Version: 3
Effective date: 2025-01-29
Source export date: 2026-10-27
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:13:21

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 · 12 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M014	openfda.application_number
brand name		Pain Be Gone	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Back to Earth Inc.	openfda.manufacturer_name
ndc	package	82721-001-01	openfda.package_ndc
ndc	package	82721-001-02	openfda.package_ndc
ndc	product	82721-001	openfda.product_ndc
ndc11	package	82721000102	derived:openfda.package_ndc
ndc11	package	82721000101	derived:openfda.package_ndc
spl id		2ce15484-38f2-014d-e063-6294a90aced2	id
spl set id		f49e718b-ef89-b648-e053-2a95a90a96c8	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

■ For external use only. ■ Avoid Contact with the eyes. If conditions worsen, or if symptoms persist for more that 7 days or clear up and occur again within a few days, discontinue use of this product and consult a physician/doctor. ■ Do not apply to wounds or damaged skin. ■ Do not bandage tightly. ■ Keep out of reach of children. In case of overdose, 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.