FDA label 0b669957-1ea3-45ff-83a4-851ee52b5e51

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)

SPL set ID: 455353d1-74dc-4b54-9da8-9ab5b81d14be
SPL ID: 0b669957-1ea3-45ff-83a4-851ee52b5e51
Version: 5
Effective date: 2014-05-21
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:29:25

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 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		0b669957-1ea3-45ff-83a4-851ee52b5e51	id
spl set id		455353d1-74dc-4b54-9da8-9ab5b81d14be	set_id

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 swallow. If Accidentally ingested, induce vomiting. Call a physician or poison control center immediately. If irritation develops, discontinue use of this product and consult a physician. Do not use on open sores, wounds, irritated or broken skin. Do not use with other creams, gels, ointments, topical medications, heating pads or other heat producing devices. Avoid contact with eyes or mucous membrane. Store in a cool dry place. Keep out of reach of children to avoid accidental poisoning. BioFlexor gel is contraindicated in patients with a known hypersensitivity to menthol. For children under 2, pregnant or nursing mothers, consult a physician .

Reported adverse events (FAERS/openFDA)#

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