Kapsin by Apipharmausa, LLC Kapsin

Kapsin by

Drug Labeling and Warnings

Kapsin by is a Otc medication manufactured, distributed, or labeled by Apipharmausa, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

KAPSIN- camphor (synthetic), capsaicin ointment 
Apipharmausa, LLC

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Kapsin

Drug Facts

Active ingredients

Camphor 3.16%

Capsaicin 0.03%

Purpose

External Analgesic

Uses

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

Warnings

For external use only.

When using this product

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

Stop use and consult a doctor if:

• condition worsens or if symptoms persist for more than 7 days
• if conditions clear up and occur again within a few days

Keep out of reach of children.

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

Directions

• Adults and children 2 years of age and older: apply to affected area not more than 3 to 4 times daily 
• Children under 2 years of age: consult a doctor

Other information

• store at 77°F (25°C)

Inactive ingredients

alcohol, chili pepper (capsicum frutescens) fruit extract, lanolin wax, petrolatum, propolis wax, water.

Package Labeling: 73061-003-60

KAPSIN 
camphor (synthetic), capsaicin ointment

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 73061-003
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	31.6 mg  in 1 g
CAPSAICIN (UNII: S07O44R1ZM) (CAPSAICIN - UNII:S07O44R1ZM)	CAPSAICIN	0.3 mg  in 1 g

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
CAPSICUM (UNII: 00UK7646FG)
PETROLATUM (UNII: 4T6H12BN9U)
PROPOLIS WAX (UNII: 6Y8XYV2NOF)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 73061-003-60	1 in 1 BOX	09/04/2020	04/01/2025
1		60 g in 1 TUBE; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	09/04/2020	04/01/2025

Labeler - Apipharmausa, LLC (117030000)

Revised: 5/2025

Document Id: 357ddece-0b27-3e50-e063-6294a90ab4ab

34390-5

Set id: 66d5c4ab-5395-4ede-8430-7c9c0e211975

Version: 4

Effective Time: 20250519