HealthWise Pain Relief Spray

Manufacturer
Veridian Healthcare | Derma Care Research Labs, LLC
Effective date
2025-10-02
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:15:33

Label at a glance#

ProductHealthWise Pain Relief
Active ingredientMENTHOL
Label structure8 sections

Indications and uses

Uses For the temporary relief of minor pain associated with • arthritis • simple backache • muscle strains • sprains • bruises

Dosage and administration

Adults and children 2 years or older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: ask a doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol 10.5%

Purpose

OTC - PURPOSE SECTION

External Analgesic

Uses

INDICATIONS & USAGE SECTION

Uses For the temporary relief of minor pain 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 or flame

When using this product

OTC - WHEN USING SECTION

When using this product

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 puncture or incinerate. Do not store at

temperature above 120ºF

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • rash or irritation develops and lasts 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 or older:Apply to affected area not more than 3 to 4 times daily.
  • Children under 2 years of age:ask a doctor.

Other information

OTHER SAFETY INFORMATION

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

Inactive ingredients

INACTIVE INGREDIENT SECTION

butylene glycol, camellia sinensis leaf extract, centella asiatica extract, chamomilla recutita (matricaria) flower extract, denatonium benzoate, dimethyl sulfone, glycyrrhiza glabra (licorice) root extract, isopropyl myristate, polygonum cuspidatum root extract, rosmarinus officinalis (rosemary) leaf extract, scutellaria baicalensis root extract, SD alcohol, water

Questions or comments?

OTC - QUESTIONS SECTION

1-888-326-1313

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71101-067-01HealthWise Pain Relief89 mL in 1 BOTTLESPRAY891

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
71101-06771101-067-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 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
HealthWise Pain ReliefMENTHOLVeridian Healthcare06be5331-7a1e-4ab3-9f17-2d350bd4b8902025-10-02WarningsExact identifier
ndc (package): 71101-067-01
ndc (product): 71101-067
ndc11 (package): 71101006701
spl id: 402d3411-8683-274a-e063-6294a90a500b
spl set id: 06be5331-7a1e-4ab3-9f17-2d350bd4b890

Reported adverse events (FAERS/openFDA)#

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