Doloflex 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: Doloflex Pain Relief
Generic name: MENTHOL, METHYL SALICYLATE
Manufacturer: United Health & Beauty Corp
Product type: HUMAN OTC DRUG
SPL set ID: 32a830cc-04d3-102e-e063-6294a90a1cad
SPL ID: 40ffa941-e0b5-3f35-e063-6394a90a9d6f
Version: 2
Effective date: 2025-10-12
Source export date: 2026-10-27
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a73bb3b6a943796a18cd4bcd0917240b579be4636d00e6e39481bafbd8093f69/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:36:37

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 · 14 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Doloflex Pain Relief	openfda.brand_name
generic name		MENTHOL, METHYL SALICYLATE	openfda.generic_name
manufacturer name		United Health & Beauty Corp	openfda.manufacturer_name
ndc	package	85350-039-11	openfda.package_ndc
ndc	package	85350-039-10	openfda.package_ndc
ndc	product	85350-039	openfda.product_ndc
ndc11	package	85350003911	derived:openfda.package_ndc
ndc11	package	85350003910	derived:openfda.package_ndc
rxcui		2711803	openfda.rxcui
spl id		40ffa941-e0b5-3f35-e063-6394a90a9d6f	id
spl set id		32a830cc-04d3-102e-e063-6294a90a1cad	set_id
unii		L7T10EIP3A	openfda.unii
unii		LAV5U5022Y	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. Do not use on children under 12 years of age, with a heating pad (may blister skin), on wounds or damaged skin. When using this product do not bandage tightly, avoid contact with the eyes or mucous membranes. Stop use and ask a doctor if excessive irritation develops, symptoms last more than 7 days or clear up and occur again within a few days, condition worsens.

Reported adverse events (FAERS/openFDA)#

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