Frankie Avalons ZERO PAIN Roll-On Pain Reliever

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: Frankie Avalons ZERO PAIN Roll-On Pain Reliever
Generic name: CAPSAICIN
Manufacturer: WHY ENTERPRISES LLC
Product type: HUMAN OTC DRUG
SPL set ID: e32acb5f-5bc3-4228-b037-6315d080f556
SPL ID: 1b120e3c-58de-2ef6-e063-6294a90ae2d6
Version: 1
Effective date: 2024-06-17
Source export date: 2026-09-28
Source partition: 8
Source file: https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:53:20

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		Frankie Avalons ZERO PAIN Roll-On Pain Reliever	openfda.brand_name
generic name		CAPSAICIN	openfda.generic_name
manufacturer name		WHY ENTERPRISES LLC	openfda.manufacturer_name
ndc	package	84413-481-00	openfda.package_ndc
ndc	product	84413-481	openfda.product_ndc
ndc11	package	84413048100	derived:openfda.package_ndc
rxcui		252006	openfda.rxcui
spl id		1b120e3c-58de-2ef6-e063-6294a90ae2d6	id
spl set id		e32acb5f-5bc3-4228-b037-6315d080f556	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. Avoid contact with the eyes. If condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days, discontinue use of this product and consult a doctor. Do not apply to wounds or damaged skin. Do not bandage tightly. Keep Out of Reach of Children

Reported adverse events (FAERS/openFDA)#

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