Tylenol Precise Nighttime 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 Nighttime Pain Relieving
Generic name
CAMPHOR, MENTHOL
Manufacturer
Kenvue Brands LLC
Product type
HUMAN OTC DRUG
SPL set ID
2ef4fe16-0820-6aad-e063-6294a90a8449
SPL ID
2ef4fe0e-abe6-4601-e063-6394a90a99f9
Version
1
Effective date
2025-02-25
Source export date
2026-09-28
Source partition
11
Source file
https://download.open.fda.gov/drug/label/drug-label-0011-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/aa96b5a2be6b394393acd0090f6948bdf99e0e8e00666f81608929c8fa83db77/drug-label-0011-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:16:12
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. When using this product avoid contact with eyes do not apply to wounds or damaged, broken or irritated skin do not bandage tightly 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. (1-800-222-1222)

Reported adverse events (FAERS/openFDA)#

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