43473-096 2.5% Menthol PAIN RELIEF GEL

Manufacturer
Nantong Health & Beyond Hygienic Products Inc.
Effective date
2026-02-05
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:37:17

Label at a glance#

Product2.5% Menthol PAIN RELIEF
Active ingredientMENTHOL, UNSPECIFIED FORM
Label structure9 sections

Indications and uses

• temporarily relieves the minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

Dosage and administration

• adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 12 years of age: ask a doctor

Storage and handling

• store at 20° to 25°C (68° to 77°F)

Label contents#

Full prescribing information#

Active ingredient (in each gram)

OTC - ACTIVE INGREDIENT SECTION

Menthol 2.5%

Purpose

OTC - PURPOSE SECTION

Topical analgesic

Uses

INDICATIONS & USAGE SECTION

• temporarily relieves the minor aches and pains of muscles and joints associated with: • simple backache • arthritis • strains • bruises • sprains

Warnings

WARNINGS SECTION

For external use only.

Do not use
• on wounds or damaged skin
• with a heating pad
• on a child under 12 years of age with arthritis-like conditions

Ask a doctor before use if you have redness over the affected area.

When using this product
• avoid contact with eyes or mucous membranes
• 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 • excessive skin irritation occurs

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of childrenIf swallowed, get medical help or contact a Poison Control Center immediately.

Directions

DOSAGE & ADMINISTRATION SECTION

• adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily • children under 12 years of age: ask a doctor

Other information

STORAGE AND HANDLING SECTION

• store at 20° to 25°C (68° to 77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cinnamomum camphora(camphor) bark oil, Carbomer, Ethylhexylglycerin, Glycerin, Isopropyl Alcohol, Methylparaben, Polysorbate 20, Propylparaben, Purified Water, Sodium Hydroxide.

SPL UNCLASSIFIED SECTION

COOLING MENTHOL FORMULA

✓ Relives back, neck & joint pain

✓ Fast-absorbing & non-greasy

Soothes sore muscles 

Mfd for and Distributed by:
Universal Distribution Center LLC
330 Applegarth Road,
Monroe Township, NJ 08831

www.universaldc.com

MADE IN CHINA

Packaging

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

2.5% Menthol PAIN RELIEF2.5% Menthol PAIN RELIEF

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
282805menthol 2.5 % Topical GelPSN1
282805menthol 0.025 MG/MG Topical GelSCD1
282805menthol 2.5 % Topical GelSY1

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
43473-096-022.5% Menthol PAIN RELIEF1 in 1 BOXGEL11
43473-096-022.5% Menthol PAIN RELIEF57 g in 1 TUBEGEL571

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
43473-09643473-096-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

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
2.5% Menthol PAIN RELIEFMENTHOLNantong Health & Beyond Hygienic Products Inc.8075ba60-772c-4d1a-8584-722bb3e539be2026-02-05WarningsExact identifier
ndc (package): 43473-096-02
ndc (product): 43473-096
ndc11 (package): 43473009602
spl id: 4a21330e-6d27-2425-e063-6294a90a021d
spl set id: 8075ba60-772c-4d1a-8584-722bb3e539be

Reported adverse events (FAERS/openFDA)#

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