Label: KATINKO PAIN AND ITCH RELIEVING (camphor- synthetic, menthol, methyl salicylate ointment
- NDC Code(s): 52241-100-03, 52241-100-10, 52241-100-30
- Packager: Greenstone Pharmaceutical Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 8, 2023
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- ACTIVE INGREDIENT
- Purpose
- Uses:
- WARNINGS
- WHEN USING
- STOP USE
- Keep out of reach of children
- DOSAGE & ADMINISTRATION
- Other Information
- Inactive Ingredients
- MANUFACTURED BY:
- PRINCIPAL DISPLAY PANEL
- 30g Package Label
-
INGREDIENTS AND APPEARANCE
KATINKO PAIN AND ITCH RELIEVING
camphor (synthetic), menthol, methyl salicylate ointmentProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:52241-100 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET) (CAMPHOR (SYNTHETIC) - UNII:5TJD82A1ET) CAMPHOR (SYNTHETIC) 11 g in 100 g MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 7.6 g in 100 g METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 13 g in 100 g Inactive Ingredients Ingredient Name Strength PETROLATUM (UNII: 4T6H12BN9U) PARAFFIN (UNII: I9O0E3H2ZE) EUCALYPTUS OIL (UNII: 2R04ONI662) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:52241-100-10 1 in 1 CARTON 05/24/2010 1 10 g in 1 JAR; Type 0: Not a Combination Product 2 NDC:52241-100-03 1 in 1 CARTON 05/24/2010 2 3 g in 1 JAR; Type 0: Not a Combination Product 3 NDC:52241-100-30 1 in 1 CARTON 05/24/2010 3 30 g in 1 BOTTLE; 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 05/24/2010 Labeler - Greenstone Pharmaceutical Inc. (719794307) Registrant - Greenstone Pharmaceutical Inc. (719794307) Establishment Name Address ID/FEI Business Operations Greenstone Pharmaceutical Inc. 719794307 manufacture(52241-100)