KATINKO EXTERNAL ANALGESIC OIL (camphor- synthetic, menthol, methyl salicylate oil

Katinko External Analgesic Oil by

Drug Labeling and Warnings

Katinko External Analgesic Oil by is a Otc medication manufactured, distributed, or labeled by Greenstone Pharmaceutical Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active ingredients

Camphor 5% Menthol 16%

Methyl salicylate 30%

Purpose

External analgesic

Use

• For the temporary relief of minor aches and pains of muscles and joints.

Warnings

For external use only

When using this product

• avoid contact with eyes or mucous membranes
• do not apply to wounds or damaged skin
• do not bandage tightly
• do not use otherwise than as directed

Stop use and ask a doctor if

• condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
• excessive irritation of the skin develops

Keep out of reach of children

If swallowed, get medical help or contact a Poison Control Center right away. to avoid accidental poisoning.

Directions

• Adults and children 3 years of age and older. Apply to affected area not more than 3 to 4 times daily
• Children under 3 years of age: Consult a doctor.

Inactive ingredients

Light Mineral Oil

Package Labeling:52241-301-01

Package Labeling:52241-301-02

INGREDIENTS AND APPEARANCE

KATINKO EXTERNAL ANALGESIC OIL 
camphor (synthetic), menthol, methyl salicylate oil

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 52241-301
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET)	CAMPHOR (SYNTHETIC)	50 mg  in 1 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	160 mg  in 1 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ)	METHYL SALICYLATE	300 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 52241-301-01	1 in 1 CARTON	06/01/2023
1		10 mL in 1 BOTTLE; Type 0: Not a Combination Product
2	NDC: 52241-301-02	1 in 1 CARTON	06/01/2023
2		35 mL in 1 BOTTLE, GLASS; 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	06/01/2023

Labeler - Greenstone Pharmaceutical Inc. (719794307)

Establishment
Name	Address	ID/FEI	Business Operations
Greenstone Pharmaceutical Inc.		719794307	manufacture(52241-301)