CRYSALO- methyl salicylate, menthol liquid

Crysalo by

Drug Labeling and Warnings

Crysalo by is a Otc medication manufactured, distributed, or labeled by V2 Pharma, LLC, A.I.G. Technologies, Inc. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Crysalo

Pain Relieving Spray

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

Methyl Salicylate 11%, Menthol 5%

Topical Analgesic

Uses

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:

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.

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:

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.

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

Instructions for using Crysalo:

• 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

Store tightly closed in a cool dry place.

INACTIVE INGREDIENT

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

INGREDIENTS AND APPEARANCE

CRYSALO 
methyl salicylate, menthol liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72835-511
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	11 g  in 100 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	5 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
ALOE VERA LEAF JUICE (UNII: RUE8E6T4NB)
PRUNUS ILICIFOLIA WHOLE (UNII: 7787172DEU)
water (UNII: 059QF0KO0R)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)
EUCALYPTUS ROBUSTA LEAF OIL (UNII: GW6X7V7NZA)
PEPPERMINT OIL (UNII: AV092KU4JH)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
SPEARMINT OIL (UNII: C3M81465G5)
GLUCOSAMINE HCL (UNII: 750W5330FY)
PEA (UNII: W4X7H8GYFM)
GLYCERIN (UNII: PDC6A3C0OX)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72835-511-01	57 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product	08/21/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved drug other		08/21/2025

Labeler - V2 Pharma, LLC (102457346)

Establishment
Name	Address	ID/FEI	Business Operations
A.I.G. Technologies, Inc		086365223	manufacture(72835-511) , label(72835-511) , pack(72835-511)