NanoX Pain Relieving Cream

Manufacturer: MG Science Technologies LLC | Chae Organics LLC
Effective date: 2026-03-12
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 01:50:04

Label at a glance#

ProductNanoX Pain Relieving

Active ingredientMENTHOL, METHYL SALICYLATE

Label structure8 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, and sprains.

Dosage and administration

Adults and children 2 years of age and older: Apply to affected areas not more than 3 to 4 times daily. Children under 2 years of age: Do not use, consult a doctor.

Contacts and useful links#

Websitewww.nanoxtreme.com

www.nanoxtreme.com

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 4%

Methyl Salicylate 10%

Purpose

OTC - PURPOSE SECTION

Cooling pain relief

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with simple backache, arthritis, strains, and sprains.

Warnings

WARNINGS SECTION

For external use only. Wash hands thoroughly before and after each use and cap bottle tightly. Flammable - Keep away from fire or flame. Avoid contact with the eyes. Do not apply to wounds or damaged skin. Do not bandage tightly.

Do not use

OTC - DO NOT USE SECTION

on reddened, damaged or sensitive skin.

If condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor

Ask a doctor before use if:

OTC - ASK DOCTOR/PHARMACIST SECTION

You are pregnant, breast feeding, have sensitive skin, are allergic to any ingredients, or are taking any prescription medications.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact the Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 2 years of age and older: Apply to affected areas not more than 3 to 4 times daily. Children under 2 years of age: Do not use, consult a doctor.

Other Information

SPL UNCLASSIFIED SECTION

When using this product: Avoid contact with mouth, nose, or genitals and be careful not to touch those areas while the cream is on your hands. Do not apply heat, heating pad or hot water. Store in a cool dry place.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Water, DMSO, Carbomer Powder, Cayenne Oil, Avocado Oil, Emu Oil, Camphor Oil, Lavender Oil, Arnica Oil, Tea tree Oil, Eucalyptus Oil, Spearmint Oil, Black Pepper Oil, Turmeric Extract, Capsicum Oleoresin, Potassium Sorbate, Sodium Benzoate.

Questions or comments:

OTC - QUESTIONS SECTION

inquiries@mgsciencetech.com

TSA Compliant

www.nanoxtreme.com

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	SPL version
2698214	menthol 4 % / methyl salicylate 10 % Topical Cream	PSN	1
2698214	menthol 40 MG/ML / methyl salicylate 100 MG/ML Topical Cream	SCD	1
2698214	menthol 4 % / methyl salicylate 10 % Topical Cream	SY	1

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
QR code link	QR Code	qr-codes.io/UtiSb5		NanoX - Label - 100ml.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
84804-322-01	NanoX Pain Relieving	100 mL in 1 TUBE	CREAM	100		1

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NanoX Pain Relieving
MENTHOL, METHYL SALICYLATE
WATER
DIMETHYL SULFOXIDE
AVOCADO OIL
EMU OIL
CAMPHOR OIL
LAVENDER OIL
TEA TREE OIL
EUCALYPTUS OIL
SPEARMINT OIL
BLACK PEPPER OIL
TURMERIC
CAPSICUM OLEORESIN
POTASSIUM SORBATE
SODIUM BENZOATE
MENTHOL
METHYL SALICYLATE
SALICYLIC ACID

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
84804-322	84804-322-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
DIMETHYL SULFOXIDE	YOW8V9698H	IACT
AVOCADO OIL	6VNO72PFC1	IACT
EMU OIL	344821WD61	IACT
CAMPHOR OIL	75IZZ8Y727	IACT
LAVENDER OIL	ZBP1YXW0H8	IACT
TEA TREE OIL	VIF565UC2G	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
SPEARMINT OIL	C3M81465G5	IACT
BLACK PEPPER OIL	U17J84S19Z	IACT
TURMERIC	856YO1Z64F	IACT
CAPSICUM OLEORESIN	UW86K581WY	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
SODIUM BENZOATE	OJ245FE5EU	IACT
MENTHOL	L7T10EIP3A	ACTIB
METHYL SALICYLATE	LAV5U5022Y	ACTIB

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
NanoX Pain Relieving	MENTHOL, METHYL SALICYLATE	MG Science Technologies LLC	4cc38927-8a8c-2df3-e063-6294a90aa0c1	2026-03-12	Warnings	Exact identifier ndc (package): 84804-322-01 ndc (product): 84804-322 ndc11 (package): 84804032201 spl id: 4cc38936-69fa-299f-e063-6294a90a9e69 spl set id: 4cc38927-8a8c-2df3-e063-6294a90aa0c1

Reported adverse events (FAERS/openFDA)#

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