Tylenol Precise Cooling Pain Relieving

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: Tylenol Precise Cooling Pain Relieving
Generic name: LIDOCAINE, MENTHOL
Manufacturer: Kenvue Brands LLC
Product type: HUMAN OTC DRUG
SPL set ID: fc0a3404-b174-3952-e053-6294a90a1e02
SPL ID: 4aeeae88-3c06-e83e-e063-6294a90aab70
Version: 5
Effective date: 2026-02-16
Source export date: 2026-09-28
Source partition: 3
Source file: https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/fd09911bd1bc81f7f2faeb048e63855fe224e494376ae919a0035190e315c050/drug-label-0003-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:19:34

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 · 18 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Tylenol Precise Cooling Pain Relieving	openfda.brand_name
generic name		LIDOCAINE, MENTHOL	openfda.generic_name
manufacturer name		Kenvue Brands LLC	openfda.manufacturer_name
ndc	package	69968-0793-1	openfda.package_ndc
ndc	package	69968-0793-9	openfda.package_ndc
ndc	package	69968-0793-4	openfda.package_ndc
ndc	package	69968-0793-2	openfda.package_ndc
ndc	product	69968-0793	openfda.product_ndc
ndc11	package	69968079302	derived:openfda.package_ndc
ndc11	package	69968079304	derived:openfda.package_ndc
ndc11	package	69968079309	derived:openfda.package_ndc
ndc11	package	69968079301	derived:openfda.package_ndc
rxcui		250912	openfda.rxcui
spl id		4aeeae88-3c06-e83e-e063-6294a90aab70	id
spl set id		fc0a3404-b174-3952-e053-6294a90a1e02	set_id
unii		98PI200987	openfda.unii
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. Do not use ▪ in large quantities, particularly over raw surfaces or blistered areas When using this product ▪ avoid contact with eyes Stop use and ask a doctor if ▪ condition worsens or symptoms persist for more than 7 days ▪ symptoms clear up and occur again within a few days Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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