PainBloc24 ProWomen Womens Discomforts Menthol Pain and Sleep Patch

Manufacturer
VIZURI HEALTH SCIENCES LLC | Shawsheen Rubber Co.
Effective date
2022-01-10
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-05-31 23:47:32

Label at a glance#

ProductPainBloc24 ProWomen Womens Discomforts Menthol Pain and Sleep Patch
Active ingredientMENTHOL
Label structure10 sections

Indications and uses

For the temporary relief of minor aches and pains of muscles and joints associated with: Simple backache Muscle strains Arthritis Bruises Sprains

Dosage and administration

Adults over 18 years: clean and dry affected area trim excessive hair for better adhesion open pouch and remove patch remove backing from patch by grasping both ends and pulling backing apart peel off one half of backing and place patch onto affected area peel off other half of backing and press and smooth onto skin use patch as needed for up to 8 hours. Do not remove when wet or directly after showering or bathin...

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Menthol unspecified 6%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of minor aches and pains of muscles and joints associated with:

  • Simple backache
  • Muscle strains
  • Arthritis
  • Bruises
  • Sprains

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • use only as directed
  • consult your doctor before use if using any medications or supplements that contain any of these same ingredients
  • do not bandage tightly
  • do not use with heating pad
  • avoid contact with eyes and mucous membranes
  • do not apply to wounds, damaged, broken or irritated skin
  • do not use at the same time as other topical analgesics

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • redness persists, spreads or becomes tender
  • symptoms last more than 7 days or clear up and occur again within a few days
  • you experience burning swelling or blistering where applied

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breast-feeding, ask a healthcare professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults over 18 years:

  • clean and dry affected area
  • trim excessive hair for better adhesion
  • open pouch and remove patch
  • remove backing from patch by grasping both ends and pulling backing apart
  • peel off one half of backing and place patch onto affected area
  • peel off other half of backing and press and smooth onto skin
  • use patch as needed for up to 8 hours. Do not remove when wet or directly after showering or bathing. Allow patch to dry and then slowly remove.
  • use one patch at a time for up to 8 hours

Children under 18 years: consult a doctor

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Acrylic adhesive, arnica montana flower extract, chamomile, d-limonene, dipropylene glycol, gamma-aminobutyric acid (GABA), hemp oil, l-theanine, lavender, magnesium chloride, melatonin, passionflower, polysorbate 80, tocopheryl acetate (Vitamin E), white curcumin

Questions

OTC - QUESTIONS SECTION

Call 855-438-3944

Other Information

SPL UNCLASSIFIED SECTION

Store in a cool, dry place at room temperature

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6bd95106-a412-1dad-b9cc-4cb74bfb27ceProduct name220230315
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
d5e51f11-ad28-caa4-4b49-4143974782adProduct name120150831
290f523a-f9db-9774-b5a9-e1f908ac1782Product name120150828
c6b65c52-69c7-df49-550a-a50c137f6218Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71226-004-012023-07-28C16284748780-10191ceaa-63a2-198a-e063-dbdaa90aec3efc79795f-25ce-4d06-88f6-5b1e4bf39815

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71226-004-01PainBloc24 ProWomen Womens Discomforts Menthol Pain and Sleep Patch5 in 1 POUCHPATCH51
71226-004-01PainBloc24 ProWomen Womens Discomforts Menthol Pain and Sleep Patch1 in 1 CARTONPATCH11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71226-004PAINBLOC24 PROWOMEN WOMENS DISCOMFORTS MENTHOL PAIN AND SLEEP PATCH (MENTHOL 6%) PATCH [VIZURI HEALTH SCIENCES LLC]1Legacy NDC, 2 package rows20220125_fc79795f-25ce-4d06-88f6-5b1e4bf39815.zip

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71226-00471226-004-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
d53fdd9a-6553-3573-e053-2995a90abeb0fc79795f-25ce-4d06-88f6-5b1e4bf398152022-01-10WarningsExact identifier
spl id: d53fdd9a-6553-3573-e053-2995a90abeb0
spl set id: fc79795f-25ce-4d06-88f6-5b1e4bf39815

Reported adverse events (FAERS/openFDA)#

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