HealthWise 16% Menthol Pain Relief Spray

Manufacturer
Veridian Healthcare | Nantong Health & Beyond Hygienic Products Inc.
Effective date
2025-12-17
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:26:39

Label at a glance#

ProductHealthWise Original Menthol
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

 for temporary relief of minor pain and associated with: arthritis simple backache muscle strains sprains bruises

Dosage and administration

adults and children 2 years and older: apply to affected area not more than 3 to 4 times daily.   children under 2 years of age: do not use, ask a doctor

Storage and handling

Store out of direct sunlight, in a cool dry well-ventilated area

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Menthol 16%

OTC - ACTIVE INGREDIENT SECTION

OTC - PURPOSE SECTION

External analgesic

Uses

INDICATIONS & USAGE SECTION

 for temporary relief of minor pain and associated with:

  • arthritis
  • simple backache
  • muscle strains
  • sprains
  • bruises

Warnings

WARNINGS SECTION

For external use only

Flammable Do not use while smoking or near heat of flame.

Stop use and ask a doctor 

OTC - ASK DOCTOR SECTION

  • condition worsens
  • rash or irritation develops and lasts for more than 7 days or clear up and occur again withing a few days

When using this product

OTC - WHEN USING SECTION

  • keep out of eyes. In case of contact with eyes, flush thoroughly with water
  • avoid contact with broken skin
  • do not bandage tightly
  • do not use with heating pad
  • contents under pressure.  Do not punture or incinerate.  Do not store at temperature above 120 F

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • rash or irritation develops and last for more than 7 days or clear up and occur again within a few days

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • adults and children 2 years and older:apply to affected area not more than 3 to 4 times daily.  
  • children under 2 years of age:do not use, ask a doctor

Other information

STORAGE AND HANDLING SECTION

  • Store out of direct sunlight, in a cool dry well-ventilated area

Inactive ingredients

INACTIVE INGREDIENT SECTION

glycerine, propylene glycol, SD alcohol, water

PRINCIPAL DISPLAY PANEL - 

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1430458menthol 16 % Topical SprayPSN2
1430458menthol 160 MG/ML Topical SpraySCD2
1430458menthol 16 % Topical SpraySY2

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71101-080-01HealthWise Original Menthol113 mL in 1 BOTTLESPRAY1132

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71101-08071101-080-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12025-11-17monthly-update2026-06-03 17:40:20

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
HealthWise Original MentholMENTHOLVeridian Healthcaree4bfb6b0-545e-4fbc-8538-4f41a6be10252025-12-17WarningsExact identifier
ndc (package): 71101-080-01
ndc (product): 71101-080
ndc11 (package): 71101008001
spl id: 46287658-1438-2401-e063-6394a90a1055
spl set id: e4bfb6b0-545e-4fbc-8538-4f41a6be1025

Reported adverse events (FAERS/openFDA)#

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