Roll Pain Away Lavender

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: Roll Pain Away Lavender
Generic name: CAPSAICIN
Manufacturer: PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA
Product type: HUMAN OTC DRUG
SPL set ID: 547ef2d9-f5c7-9de1-e063-6394a90a218b
SPL ID: 547ef489-1152-e473-e063-6394a90a3dbf
Version: 1
Effective date: 2026-06-17
Source export date: 2026-09-28
Source partition: 14
Source file: https://download.open.fda.gov/drug/label/drug-label-0014-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/db99fd80353afecef4949b48edcaa018be72b966b2360184251eb14df43743f9/drug-label-0014-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:39:59

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		Roll Pain Away Lavender	openfda.brand_name
generic name		CAPSAICIN	openfda.generic_name
manufacturer name		PROXIMITY CAPITAL PARTNERS LLC DBA ASUTRA	openfda.manufacturer_name
ndc	package	72683-010-01	openfda.package_ndc
ndc	product	72683-010	openfda.product_ndc
ndc11	package	72683001001	derived:openfda.package_ndc
rxcui		199870	openfda.rxcui
spl id		547ef489-1152-e473-e063-6394a90a3dbf	id
spl set id		547ef2d9-f5c7-9de1-e063-6394a90a218b	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 Use only as directed. For external use only. When using this product: avoid contact with eyes do not apply to wounds or damaged skin do not bandage tightly Stop use and ask doctor if: condition worsens symptoms persist for more than 7 days, or clear up and reoccur again within a few days redness is present irritation develops If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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