DR-HO'S PAIN RELIEF SPRAY MAXIMUM STRENGTH 4 FL OZ (120 mL)

Manufacturer
LABORATOIRES DRUIDE INC
Effective date
2022-02-11
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 22:08:47

Label at a glance#

ProductDR HOS PAIN RELIEF MAXIMUM STRENGTH
Active ingredientMENTHOL
Label structure12 sections

Indications and uses

■ for the temporary relief of minor aches and pains of muscles and joints.

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 of age : consult a physician. ■ Shake well before usage. ■ Simply spray solution on affected body part and let penetrate through skin while gently rubbing. ■ Storage information: store at room temperature. ■ Close cap tightly after use.

Label contents#

Full prescribing information#

Active Ingredient (In each spray)

OTC - ACTIVE INGREDIENT SECTION

Menthol 3.00%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

■ for the temporary relief of minor aches and pains of muscles and joints.

Warnings

WARNINGS SECTION

■ For external use only.

■ Avoid contact with eyes and mucous membranes.

■ Do not apply on wounds or damaged skin.

■ Do not bandage tightly.

■ Do not apply external heat such us an electric heating pad, as this may result in excessive skin irritation or skin burn.

■ Do not apply on or near the nipple.

■ If pregnant or breastfeeding, ask a health professional before use.

■ Do not inhale or swallow.

■ Allergy Alert: Do not use if allergic to Asteraceae/Compositae/Daisy family or to any other ingredient contained in this product.

■ Flammable: Keep away from fire or flame.

When using this product

OTC - DO NOT USE SECTION

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

Stop use and ask a doctor

OTC - STOP USE SECTION

if condition worsens or if symptoms persist for more than seven days or clear up and occur again within a few days.

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

■ Adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily. Children under 12 of age: consult a physician.

■ Shake well before usage.

■ Simply spray solution on affected body part and let penetrate through skin while gently rubbing.

■ Storage information: store at room temperature.

■ Close cap tightly after use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Alcohol, Arnica Montana Flower Extract, Mineral Oil, Dimethicone, Laureth-2, Sodium Stearoyl Glutamate, Castor Oil, Aloe Barbadensis Leaf Juice, Tocopherol (Vitamin E), Linoleic Acid (and) Linolenic Acid (Vitamin F).

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 SPRAY MAXIMUM STRENGTH 120 mL (NDC 71447-122-00)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Dr Ho's Pain Relief Spray 120 mLDr Ho's Pain Relief Spray 120 mL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71447-122-012024-01-30C16284748780-11030e365-423e-111a-e063-dadaa90a10e2DR-HO'S PAIN RELIEF SPRAY MAXIMUM STRENGTH 4 FL OZ (120 mL)

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
71447-12271447-122-00, 71447-122-01

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
d7c12015-dca1-4ab1-e053-2a95a90a480cd7c12015-dca0-4ab1-e053-2a95a90a480c2022-02-11WarningsExact identifier
spl id: d7c12015-dca1-4ab1-e053-2a95a90a480c
spl set id: d7c12015-dca0-4ab1-e053-2a95a90a480c

Reported adverse events (FAERS/openFDA)#

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