FDA.reportPublic FDA data

Dr Kevin Khalili Pain Relief Cream

Manufacturer
DR. KHALILI LLC
Effective date
2025-07-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:08:06

Label at a glance#

ProductDr Kevin Khalili Pain Relief Cream
Active ingredientMENTHOL
Label structure7 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, muscle strains, bruises and joint sprains

Dosage and administration

Shake tube prior to each use. Use only as directed. Adults and children over 12 years: Apply to affected areas not more than 2 times a day. Massage into painful areas until thoroughly absorbed into skin. Wash hands with soap and Store a 21/102 water after each use. Store at 21° to 24°C (69° to 78°F). Children 12 years or younger: Ask a doctor.

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Menthol 6%

PURPOSE

OTC - PURPOSE SECTION

.Topical analgesic

USES

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with: arthritis, simple backache, muscle strains, bruises and joint sprains

WARNINGS

WARNINGS SECTION

For external use only.

When using this product

OTC - WHEN USING SECTION

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

OTC - STOP USE SECTION

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

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a doctor before use.

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

In case of accidental ingestion, seek immediate medical assistance or contact poison control.

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Shake tube prior to each use. Use only as directed.

Adults and children over 12 years: Apply to affected areas not more than 2 times a day. Massage into painful areas until thoroughly absorbed into skin. Wash hands with soap and Store a 21/102

water after each use. Store at 21° to 24°C (69° to 78°F).

Children 12 years or younger: Ask a doctor.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

DI Water, Aloe Leat Juice, Dimethyl Sulfone (MSM), Virgin Coconut Oil, Avocado Oil, Jojoba Seed Oil, Glyceryl Stearate

SE (Vegetable), Vegetable Emulsifying Vegetable Glycerin, Camphor, Arnica Flower Extract, Comfrey Extract, Ginger Root Extract, Cayenne Pepper Extract, Oregano Leaf Extract, Thyme Flower/Leaf Extract, Cinnamon Bark Extract, Rosemary Leaf Extract, Lavender Flower Extract, Golden Seal Root Extract, Proprietary Aroma (Botanical Based Blend), Cetyl Hydroxyethylcellulose (Tree Bark), Boswellia Carterii Oil, Tetrahydrocurcuminoids (Curcumin), Squalane (Olive), Stearic Acid (Vegetable), Citric Acid (Fruit), Tetrahydropiperine (Black Pepper)

Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1488306menthol 6 % Topical CreamPSN2
1488306menthol 60 MG/ML Topical CreamSCD2
1488306menthol 6 % Topical CreamSY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
85953-001-90Dr Kevin Khalili Pain Relief Cream90 g in 1 TUBECREAM902

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 32 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
85953-00185953-001-90

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Name, UNII, Kind table
NameUNIIKind
LAVENDER OILZBP1YXW0H8IACT
GOLDENSEALZW3Z11D0JVIACT
COMFREYD05HXK6R3GIACT
CETYL HYDROXYETHYLCELLULOSE (350000 MW)T7SWE4S2TTIACT
STEARETH-20L0Q8IK9E08IACT
CINNAMON OILE5GY4I6YCZIACT
CETEARYL ALCOHOL2DMT128M1SIACT
PEG-150 STEARATE7BSG7DF10QIACT
GLYCERINPDC6A3C0OXIACT
ARNICA MONTANA FLOWEROZ0E5Y15PZIACT
GINGERC5529G5JPQIACT
CURCUMINIT942ZTH98IACT
ALOE BARBADENSIS LEAF JUICERUE8E6T4NBIACT
AVOCADO OIL6VNO72PFC1IACT
JOJOBA OIL724GKU717MIACT
GLYCERYL STEARATE230OU9XXE4IACT
POLYSORBATE 60CAL22UVI4MIACT
CAMPHOR OIL75IZZ8Y727IACT
THYMECW657OBU4NIACT
SQUALANEGW89575KF9IACT
STEARIC ACID4ELV7Z65APIACT
CITRIC ACID2968PHW8QPIACT
TETRAHYDROPIPERINE8904DO502TIACT
WATER059QF0KO0RIACT
DIMETHYL SULFONE9H4PO4Z4FTIACT
OREGANO0E5AT8T16UIACT
BOSWELLIA CARTERII OIL67ZYA5T02KIACT
COCONUT OILQ9L0O73W7LIACT
CAPSICUM ANNUUM WHOLE7FKZ3QQQ1FIACT
ROSEMARY OIL8LGU7VM393IACT
MENTHOLL7T10EIP3AACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Dr Kevin Khalili Pain Relief CreamMENTHOLDR. KHALILI LLC3a79b38c-9adc-60dd-e063-6394a90a5b302025-07-21WarningsExact identifier
ndc (package): 85953-001-90
ndc (product): 85953-001
ndc11 (package): 85953000190
spl id: 3a79877f-35d6-c08b-e063-6294a90a86f5
spl set id: 3a79b38c-9adc-60dd-e063-6394a90a5b30

Reported adverse events (FAERS/openFDA)#

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