DR HO S PAIN RELIEF EXTRA STGHT

Manufacturer
LABORATOIRES DRUIDE INC
Effective date
2023-02-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:36:08

Label at a glance#

ProductDR HO S PAIN RELIEF EXTRA STGHT
Active ingredientMETHYL SALICYLATE, MENTHOL, EUCALYPTUS OIL
Label structure12 sections

Indications and uses

■ Provides temporary soothing relief of sore muscles associated with strains and sprains, backaches, lumbago, pain of tendons and or ligaments as well as arthritic or rheumatic pain.

Dosage and administration

■ For use on adults and children over 12 years of age. ■ Apply generously to the affected area using hands-free applicator ■ Use 3 to 4 times per day as required. A stinging or burning sensation will be experienced during the first few minutes as the formula begins working. For arthritis or muscle pain of the hands, retain for at least 10 minutes then wash hands.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Methyl Salicylate 30%

Menthol 15.00%

Eucalyptus Oil 1%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

USES

INDICATIONS & USAGE SECTION

■ Provides temporary soothing relief of sore muscles associated with strains and sprains, backaches, lumbago, pain of tendons and or ligaments as well as arthritic or rheumatic pain.

WARNINGS

WARNINGS SECTION

■ For external use only.

■ The application of external heat may cause skin irritation or burn.

■ Avoid contact with eyes and broken skin. Do not bandage.

■ DO NOT USE IF ALLERGIC TO SALICYLATES OR IF TAKING ANTICOAGULANT MEDICATIONS.

When using this product

OTC - DO NOT USE SECTION

rashes and or burning discomfort have been known to occur; in which case discontinue use.

■ The application of external heat may cause skin irritation or burn.

Stop use and ask a doctor

OTC - STOP USE SECTION

if condition worsens, rash or irritation develops, or if symptoms persist for more than 7 days or clear up and recur in a few days.

■ IF PREGNANT OF BREAST-FEEDING, ask a health professional before use.

Keep safely out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

■ For use on adults and children over 12 years of age.

■ Apply generously to the affected area using hands-free applicator ■ Use 3 to 4 times per day as required. A stinging or burning sensation will be experienced during the first few minutes as the formula begins working. For arthritis or muscle pain of the hands, retain for at least 10 minutes then wash hands.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Paraffin wax, Butyrospermum Parkii (Shea) Butter, Cocos Nucifera (Coconut) Oil, Tocopherol.

Questions or Comments?

OTC - QUESTIONS SECTION

1-877-374-6669 or visit www.drhonow.com

Distributed by

SPL UNCLASSIFIED SECTION

VGH Solutions Inc
150 Stewart Parkway
Greensboro, GA 30642

MADE IN CANADA

DR-HO'S PAIN RELIEF STICK EXTRA STRENGHT 1.86 OZ (53G) (NDC 71447-187-00)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

DR-HO'S PAIN RELIEF STICK EXTRA STRENGHT 1.86 OZ (53G)DR-HO'S PAIN RELIEF STICK EXTRA STRENGHT 1.86 OZ (53G)

Products#

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DailyMed product names page 1 of 1 · 10 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71447-18771447-187-00, 71447-187-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
f4b4972c-f9b9-1f25-e053-2995a90a0ca6f4b4972c-f9b8-1f25-e053-2995a90a0ca62023-02-08WarningsExact identifier
spl id: f4b4972c-f9b9-1f25-e053-2995a90a0ca6
spl set id: f4b4972c-f9b8-1f25-e053-2995a90a0ca6

Reported adverse events (FAERS/openFDA)#

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