SMOOTH GATOR Head-Ezz Analgesic

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: SMOOTH GATOR Head-Ezz Analgesic
Generic name: MENTHOL
Manufacturer: Smooth Gator LLC
Product type: HUMAN OTC DRUG
SPL set ID: 02e18e5d-6fb0-4ebf-bdd6-dcc7edbb31bd
SPL ID: 1a820f59-518c-a238-e063-6294a90a1d1f
Version: 1
Effective date: 2024-06-10
Source export date: 2026-11-06
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/2026-11-06/f699a9578a0c5d6f5abd59491e85ce3c2c5e4567a51003fee350566c56ba5812/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
Import run: 20261106T075659Z
Imported at: 2026-11-06 08:30:23

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		SMOOTH GATOR Head-Ezz Analgesic	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		Smooth Gator LLC	openfda.manufacturer_name
ndc	package	70673-501-00	openfda.package_ndc
ndc	product	70673-501	openfda.product_ndc
ndc11	package	70673050100	derived:openfda.package_ndc
rxcui		1442261	openfda.rxcui
spl id		1a820f59-518c-a238-e063-6294a90a1d1f	id
spl set id		02e18e5d-6fb0-4ebf-bdd6-dcc7edbb31bd	set_id
unii		L7T10EIP3A	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 eyes. If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do not apply to wounds or damaged skin. Do not bandage tightly.

Reported adverse events (FAERS/openFDA)#

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