BIOSAVIA External Analgesic 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: BIOSAVIA External Analgesic Pain Relief
Generic name: CAPSAICIN
Manufacturer: BIOSAVIA USA, LLC
Product type: HUMAN OTC DRUG
SPL set ID: 814aa66b-7719-4a29-a84e-18290367e9c7
SPL ID: 20ba72da-a0c4-0f35-e063-6394a90af8e8
Version: 1
Effective date: 2024-08-28
Source export date: 2026-09-28
Source partition: 5
Source file: https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:27:57

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		BIOSAVIA External Analgesic Pain Relief	openfda.brand_name
generic name		CAPSAICIN	openfda.generic_name
manufacturer name		BIOSAVIA USA, LLC	openfda.manufacturer_name
ndc	package	84680-529-00	openfda.package_ndc
ndc	product	84680-529	openfda.product_ndc
ndc11	package	84680052900	derived:openfda.package_ndc
rxcui		199870	openfda.rxcui
spl id		20ba72da-a0c4-0f35-e063-6394a90af8e8	id
spl set id		814aa66b-7719-4a29-a84e-18290367e9c7	set_id
unii		S07O44R1ZM	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 wounds or damaged skin use if you are allergic to any ingredients in this product When using this product Avoid contact with the eyes Stop use and ask a doctor if symptoms persist or get worse after than 7days swallowed If pregnant or breast-feeding, ask a health professional before use keep out reach of children

Reported adverse events (FAERS/openFDA)#

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