Katinko Pain And Itch Relieving Ointment

Manufacturer
Greenstone Pharmaceutical Inc.
Effective date
2023-12-08
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-06-01 00:03:49

Label at a glance#

ProductKatinko Pain And Itch Relieving
Active ingredientCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE
Label structure13 sections

Indications and uses

For temporary relief of minor aches and pains of muscles and joints associated with: Simple Backache       Arthritis      Rheumatism      Muscle Strain      Sprains      Bruises For temporary relief of pain and itching associated with: Insect Bites      Minor skin irritation

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients:           

Camphor 11 percent                 

Menthol 7.6 percent                 

Methyl Salicylate 13.0 percent  

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Topical Analgesic

Topical Analgesic

Uses:

INDICATIONS & USAGE SECTION

For temporary relief of minor aches and pains of muscles and joints associated with:

Simple Backache       Arthritis      Rheumatism      Muscle Strain      Sprains      Bruises

For temporary relief of pain and itching associated with:

Insect Bites      Minor skin irritation

WARNINGS SECTION

Warnings

For External Use Only.

OTC - WHEN USING SECTION

When using this product:

Use only as directed.

Do not apply to wounds or damaged skin.

Do not use on the eyes or on the mucous membranes.

Do not use with a heating pad or apply external heat.

OTC - STOP USE SECTION

Stop use and ask a doctor if:

Skin redness or excessive irritation of the skin occurs

Condition worsens

Symptoms persists for more than 7 days or clears up and occurs again within a few days

Do not bandage tightly

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a poison control

DOSAGE & ADMINISTRATION SECTION

Directions:

Adults and children 2 yrs and up              Apply to affected areas not more than 3 to 4 times daily

Children under 2 years                             Consult a doctor before use

Other Information

ADVERSE REACTIONS SECTION

This product make provoke allergic reaction in some individuals. Test on small area before use.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Petroleum Jelly, Paraffin Wax

MANUFACTURED BY:

SPL UNCLASSIFIED SECTION

Greenstone

Pharmaceutical

H.K. Inc.

Anabu Industrial Estate,

Imus, Cavite, Philippines 4103

PRODUCT O F THE PHI L I P PI N E S

MEDICATED

For external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

10g stickers10g stickers10g box10g box

30g Package Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

30g Label30g Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1542816camphor 11 % / menthol 7.6 % / methyl salicylate 13 % Topical OintmentPSN8
1542818Katinko (camphor 11 % / menthol 7.6 % / methyl salicylate 13 % ) Topical OintmentPSN8
1542818camphor 0.11 MG/MG / menthol 0.076 MG/MG / methyl salicylate 0.13 MG/MG Topical Ointment [Katinko]SBD8
1542816camphor 0.11 MG/MG / menthol 0.076 MG/MG / methyl salicylate 0.13 MG/MG Topical OintmentSCD8
1542818Katinko (camphor 11 % / menthol 7.6 % / methyl salicylate 13 % ) Topical OintmentSY8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
52241-100-03Katinko Pain And Itch Relieving1 in 1 CARTONOINTMENT18
52241-100-03Katinko Pain And Itch Relieving3 g in 1 JAROINTMENT38
52241-100-10Katinko Pain And Itch Relieving1 in 1 CARTONOINTMENT18
52241-100-10Katinko Pain And Itch Relieving10 g in 1 JAROINTMENT108
52241-100-30Katinko Pain And Itch Relieving30 g in 1 BOTTLEOINTMENT308
52241-100-30Katinko Pain And Itch Relieving1 in 1 CARTONOINTMENT18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
52241-100KATINKO PAIN AND ITCH RELIEVING (CAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATE) OINTMENT [GREENSTONE PHARMACEUTICAL INC.]8Current NDC, Legacy NDC, 6 package rows20231210_fe907fa4-4a01-4974-b71f-9cd980b4eaa2.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CAMPHOR (SYNTHETIC)ACTIVE INGREDIENT5TJD82A1ET2
MENTHOLACTIVE INGREDIENTL7T10EIP3A2
METHYL SALICYLATEACTIVE INGREDIENTLAV5U5022Y2
CAMPHOR (SYNTHETIC)ACTIVE MOIETY5TJD82A1ET2
MENTHOLACTIVE MOIETYL7T10EIP3A2
SALICYLIC ACIDACTIVE MOIETYO414PZ4LPZ2
PARAFFININACTIVE INGREDIENTI9O0E3H2ZE2
PETROLATUMINACTIVE INGREDIENT4T6H12BN9U2

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
52241-10052241-100-10, 52241-100-03, 52241-100-30

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 6 matching rows.

Source Document#

Source XML · Source PDF

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 8 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PETROLATUMPETROLATUM4T6H12BN9UOINTMENT / TOPICAL7275 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates
PARAFFINPARAFFINI9O0E3H2ZEOINTMENT / TOPICAL2860 mgExact identifier — unii+route+dosage form
4 equally ranked IID candidates

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Katinko Pain And Itch RelievingCAMPHOR (SYNTHETIC), MENTHOL, METHYL SALICYLATEGreenstone Pharmaceutical Inc.fe907fa4-4a01-4974-b71f-9cd980b4eaa22023-12-08Warnings, Adverse reactionsExact identifier
ndc (package): 52241-100-10
ndc (package): 52241-100-03
ndc (package): 52241-100-30
ndc (product): 52241-100
ndc11 (package): 52241010030
ndc11 (package): 52241010003
ndc11 (package): 52241010010
spl id: 0c0d4eac-3530-250d-e063-6294a90aad14
spl set id: fe907fa4-4a01-4974-b71f-9cd980b4eaa2

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.