Dr Kevin Khalili Pain Relief Cream

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: Dr Kevin Khalili Pain Relief Cream
Generic name: MENTHOL
Manufacturer: DR. KHALILI LLC
Product type: HUMAN OTC DRUG
SPL set ID: 3a79b38c-9adc-60dd-e063-6394a90a5b30
SPL ID: 3a79877f-35d6-c08b-e063-6294a90a86f5
Version: 2
Effective date: 2025-07-21
Source export date: 2026-10-27
Source partition: 9
Source file: https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-27/a73bb3b6a943796a18cd4bcd0917240b579be4636d00e6e39481bafbd8093f69/drug-label-0009-of-0014.json.zip
Source manifest SHA-256: 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
Import run: 20261027T193451Z
Imported at: 2026-10-27 20:36:11

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		Dr Kevin Khalili Pain Relief Cream	openfda.brand_name
generic name		MENTHOL	openfda.generic_name
manufacturer name		DR. KHALILI LLC	openfda.manufacturer_name
ndc	package	85953-001-90	openfda.package_ndc
ndc	product	85953-001	openfda.product_ndc
ndc11	package	85953000190	derived:openfda.package_ndc
rxcui		1488306	openfda.rxcui
spl id		3a79877f-35d6-c08b-e063-6294a90a86f5	id
spl set id		3a79b38c-9adc-60dd-e063-6394a90a5b30	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. When using this product use only as directed • avoid contact with eyes, wounds, contact lenses, damaged skin or mucous membranes • do not bandage tightly or use with heat • avoid hot tub, steam room and Stop use and ask doctor if condition worsens • symptoms persist for more than 7 days or clear up and occur again within a few days • skin irritation or redness develops. If pregnant or breast-feeding ask a doctor before use. Keep out of reach of children In case of accidental ingestion, seek immediate medical assistance or contact poison control.

Reported adverse events (FAERS/openFDA)#

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