SUPER WHITE STUFF 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: SUPER WHITE STUFF Pain Relief
Generic name: MENTHOL
Manufacturer: BLUE SPRING WELLNESS
Product type: HUMAN OTC DRUG
SPL set ID: e6d27df5-118c-4c6d-86e8-7b4401a39c76
SPL ID: 0f9cff32-4c60-e95a-e063-6294a90a9707
Version: 1
Effective date: 2024-01-23
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 05:17:53

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		SUPER WHITE STUFF Pain Relief	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		BLUE SPRING WELLNESS	openfda.manufacturer_name
ndc	package	14448-445-00	openfda.package_ndc
ndc	product	14448-445	openfda.product_ndc
ndc11	package	14448044500	derived:openfda.package_ndc
rxcui		2391332	openfda.rxcui
spl id		0f9cff32-4c60-e95a-e063-6294a90a9707	id
spl set id		e6d27df5-118c-4c6d-86e8-7b4401a39c76	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 if arthritis conditions are present. For all other listed uses, consult a doctor before use on children under 2. Keep out of reach of children. If swallowed, get medical help or contact a Posion Control Center right away.

Reported adverse events (FAERS/openFDA)#

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