ZESTAMA- capsaicin liquid

Zestama by

Drug Labeling and Warnings

Zestama by is a Otc medication manufactured, distributed, or labeled by V2 Pharma LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Zestama

Touch free pain relief

Capsaicin 0.075%

External analgesic

Uses

Temporarily relieves minor aches and pains of muscles and joints associated with:

• simple backache
• arthritis 
• strains
• sprains
• bruises

DirectionsAdults and children 12 years of age and older:

Apply Zestama using the touch free roll-on applicator to affected area liberally as needed for pain. Do not use more than 4 times per day. 

For children under 12 years of age, ask a doctor.

Fore external use only

Read all warnings and directions before use. 

Test first on small area of skin. 

When using this product you may experience a burning sensation and/or skin redness. The intensity of this reaction varies among individuals and may be severe. With regular use, this generally disappears after several days.

Do not use:

• Near the face, eyes, or genetalia 
• Immediately before or after bathing or swimming
• On wounds or damaged skin
• If you are allergic to capsicum or chili peppers
• Do not bandage

Stop use and ask a doctor or pharmacist if:

• Condition worsens or does not improve after regular use
• Severe burning persists or blistering occurs
• Treated area skin begins to scale or peel as if burnt

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

Instructions for Zestama Touch Free Pain Relief:

• Lightly shake and invert bottle to allow product into applicator.
• Remove cap to expose applicator. Try not to touch any surfaces or liquids.
• Avoid contact with the eyes, lips, nose, genetalia and other mucous membranes.
• Invert the bottle, then apply liberally to affected area 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.
• Do not swim or bathe for at least 1 hour.
• Do not tightly wrap or bandage the treated area
• Do not apply heat to the treated area immediately before or after use.
• Moisture and sweat can further “activate” the treated area and warm up more

STORAGE AND HANDLING

Store tightly closed in a cool dry place. 

INACTIVE INGREDIENT

Water
Dimethicone
Alcohol
Dimethyl Sulfoxide
Lavender Oil
Decyl Glucoside
Ginger Extract
Bamboo Extract
Pea Extract
Glucosamine HCI
Arnica Extract
Propylene Glycol
Phenoxyethanol
Ethylhexylglycerin
Hydroxyethyl Cellulose
Allantoin
Echinacea Extract
Aloe Barbadensis Leaf Extract
Disodium EDTA

SPL UNCLASSIFIED SECTION

Manufactured for:

V2 Pharma, LLC

103 W Main Street

Hudson, MI 49247

Packaging for Zestama is shown below

INGREDIENTS AND APPEARANCE

ZESTAMA 
capsaicin liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 72835-175
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.075 g  in 100 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
DIMETHICONE (UNII: 92RU3N3Y1O)
ALCOHOL (UNII: 3K9958V90M)
DIMETHYL SULFOXIDE (UNII: YOW8V9698H)
LAVENDER OIL (UNII: ZBP1YXW0H8)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
GINGER (UNII: C5529G5JPQ)
BAMBUSA VULGARIS TOP (UNII: FIW80T6P6V)
PEA (UNII: W4X7H8GYFM)
GLUCOSAMINE HCL (UNII: 750W5330FY)
ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
PHENOXYETHANOL (UNII: HIE492ZZ3T)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
HYDROXYETHYL CELLULOSE (5500 MPA.S AT 2%) (UNII: M825OX60H9)
ALLANTOIN (UNII: 344S277G0Z)
ECHINACEA PURPUREA ROOT (UNII: OS64WTR4KU)
ALOE BARBADENSIS LEAF (UNII: ZY81Z83H0X)
EDETATE DISODIUM (UNII: 7FLD91C86K)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 72835-175-01	89 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product	04/01/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	04/01/2025

Labeler - V2 Pharma LLC (102457346)

Establishment
Name	Address	ID/FEI	Business Operations
V2 Pharma LLC		102457346	manufacture(72835-175) , label(72835-175)