MUSCLESHOK Sport Gel

Manufacturer
Wagner Solutions, LLC
Effective date
2018-06-08
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 00:54:47

Label at a glance#

ProductMUSCLESHOK Sport
Active ingredientHISTAMINE DIHYDROCHLORIDE
Label structure7 sections

Indications and uses

for the temporary relief of minor aches and pains of muscles and joints associated with sprains, strains, bruises, arthritis & simple backache

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; consult a doctor

Label contents#

Full prescribing information#

Active Ingredients

OTC - ACTIVE INGREDIENT SECTION

Histamine dihydrochloride 0.025%

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 sprains, strains, bruises, arthritis & simple backache

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

  • do not bandage tightly
  • do not apply to wounds or damaged skin
  • avoid contact with eyes or mucous membranes

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • condition worsens
  • symptoms persist 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 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; consult a doctor

Other Information

SPL UNCLASSIFIED SECTION

store at room temperature

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aloe Barbadensis (Aloe Vera) Leaf Juice, Arnica Montana Extract, Boswellia Serrata Extract, Carbomer, Ethylhexylglycerin, Methylsulfonylmethane (MSM), Phenoxyethanol, Triethanolamine, Water (Aqua)

Package Labeling:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130868253000426GTIN-13: 0868253000426
EAN-13: 0868253000426
GTIN-12: 868253000426
UPC-A: 868253000426
GTIN storage (14 digits): 00868253000426
Label.jpg

Products#

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

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72378-34772378-347-00

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 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
07430632-613e-01fa-e063-6294a90a25c84357b880-73ae-4e62-a343-b511a0f460642023-10-09WarningsExact identifier
spl set id: 4357b880-73ae-4e62-a343-b511a0f46064

Reported adverse events (FAERS/openFDA)#

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