BLUESPRING Doctors Pain Formula 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: BLUESPRING Doctors Pain Formula Pain Relief
Generic name: MENTHOL
Manufacturer: ACA MANAGEMENT LLC
Product type: HUMAN OTC DRUG
SPL set ID: 98f3f719-792f-4a93-95b1-90072e0f8bf4
SPL ID: 39e0ad70-7af0-cd09-e063-6394a90a0f22
Version: 1
Effective date: 2025-07-14
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:18:31

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		BLUESPRING Doctors Pain Formula Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		ACA MANAGEMENT LLC	openfda.manufacturer_name
ndc	package	83591-629-00	openfda.package_ndc
ndc	product	83591-629	openfda.product_ndc
ndc11	package	83591062900	derived:openfda.package_ndc
rxcui		2391332	openfda.rxcui
spl id		39e0ad70-7af0-cd09-e063-6394a90a0f22	id
spl set id		98f3f719-792f-4a93-95b1-90072e0f8bf4	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 wounded, damaged or irritated skin. When using this product avoid contact with eyes or mucous membranes. Do not bandage tightly Stop use and ask a doctor if you experience a rash and/or a reaction condition worsens or if symptoms persist for more than 10 days or clear up and occur again within few days. If Pregnant or Breast-Feeding ask a health professional before use. Consult a doctor before use on children under 12 years of age if arthritis conditions are present. For all other listed uses, consult a doctor before use on children under 2 years of age. 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.