Crysalo

Manufacturer
V2 Pharma, LLC
Effective date
2026-07-06
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
weekly-update
Hydrated at
2026-07-17 21:43:37

Label at a glance#

ProductCrysalo
Active ingredientMETHYL SALICYLATE, MENTHOL
Label structure10 sections

Indications and uses

Temporary relief of minor aches and pains associated with: Simple backache Arthritis Strains, sprains, and bruises

Dosage and administration

Apply to affected area not more then 3 to 4 times daily. No need to rub in. For children under 12 years of age: Ask a doctor.

Storage and handling

Store tightly closed in a cool dry place.

Label contents#

Full prescribing information#

Crysalo

SPL UNCLASSIFIED SECTION

Pain Relieving Spray

Crysalo should be administered under the supervision of a licensed medical practitioner.

Uses

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains associated with:

  • Simple backache
  • Arthritis
  • Strains, sprains, and bruises

DirectionsAdults and children 12 years of age and older:

DOSAGE & ADMINISTRATION SECTION

Apply to affected area not more then 3 to 4 times daily.
No need to rub in.
For children under 12 years of age: Ask a doctor.

Fore external use only. Avoid contact with the eyes.Keep out of reach of children.

WARNINGS SECTION

When using this product
Do not apply to wounds or damaged skin. Do not bandage tightly. Do not use with heating pad. Rinse with soap and water to remove. Wash hands with soap and water after use.

Stop use and ask doctor if:

OTC - STOP USE SECTION

Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Discontinue use of this product and consult a physician.

Instructions for using Crysalo:

INSTRUCTIONS FOR USE SECTION

  • Remove cap to expose spray applicator.
  • Avoid contact with the eyes, lips, nose, genetalia and other mucous membranes.
  • Hold spray bottle close (2-3 inches) to affected area and apply liberally 3 to 4 times daily.
  • Do not use hands to rub in.
  • Place cap back on and Wash hands thoroughly with soap and water.
  • Allow treated area to dry naturally for best results.

STORAGE AND HANDLING SECTION

Store tightly closed in a cool dry place.

INACTIVE INGREDIENT SECTION

SD Alcohol 40-B, Water, Aloe Barbadensis Leaf Extract, Spearmint Oil, Glycerin, Holly Extract, Arnica Extract, Propylene Glycol, Pea Extract, Bamboo Extract, Peppermint Oil, Camphor, Eucalyptus Oil, Glucosamine HCl, Dimethyl Sulfoxide.

SPL UNCLASSIFIED SECTION

Manufactured for:
V2 Pharma, LLC
103 W Main Street
Hudson, MI 49247

Questions or concerns call 1-(800)-519-8334

Packaging for Crysalo is shown below

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Crysalo LabelCrysalo LabelCrysalo LabelCrysalo Label

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
72835-511-01ML - Milliliter72835-51149d53c89-1db1-4934-a44a-80ef15fde99712025-10-14

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
72835-51172835-511-01

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 17 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
22025-08-28full-release2026-06-01 01:12:12

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
CrysaloMETHYL SALICYLATE, MENTHOLV2 Pharma, LLCd6c475f0-1098-41cd-868a-a5e528a5e5ae2026-07-06WarningsExact identifier
ndc (package): 72835-511-01
ndc (product): 72835-511
ndc11 (package): 72835051101
spl id: 8cba42b5-6ae5-410a-aa77-69b2ccd05860
spl set id: d6c475f0-1098-41cd-868a-a5e528a5e5ae

Reported adverse events (FAERS/openFDA)#

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