BlueStop Max

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: BlueStop Max
Generic name: EXTERNAL ANALGESIC
Manufacturer: Clavel Corporation
Product type: HUMAN OTC DRUG
SPL set ID: f2277e27-868b-57ef-e053-2a95a90abf28
SPL ID: 4835e6a9-c202-02eb-e063-6294a90a7ead
Version: 3
Effective date: 2026-01-12
Source export date: 2026-09-28
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/c7ca0b7091cdaeab3f27713a6eef00adcf8fe722383633ddce61531b4c840544/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:25:50

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		M017	openfda.application_number
brand name		BlueStop Max	openfda.brand_name
generic name		EXTERNAL ANALGESIC	openfda.generic_name
manufacturer name		Clavel Corporation	openfda.manufacturer_name
ndc	package	82714-002-01	openfda.package_ndc
ndc	product	82714-002	openfda.product_ndc
ndc11	package	82714000201	derived:openfda.package_ndc
rxcui		1595624	openfda.rxcui
spl id		4835e6a9-c202-02eb-e063-6294a90a7ead	id
spl set id		f2277e27-868b-57ef-e053-2a95a90abf28	set_id
unii		C6B1OE8P3W	openfda.unii
unii		V13007Z41A	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 When using this product: avoid contact with the eyes Stop use and ask a doctor if: condition worsens, or symptoms persist for more than 7 days or clear up and occur again within a few days 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.