FDA.reportPublic FDA data

KINKAN

Manufacturer
KINKANDO CO., LTD .
Effective date
2025-10-21
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 01:42:45

Label at a glance#

ProductKINKAN
Active ingredientAMMONIA, CAMPHOR (NATURAL), MENTHOL
Label structure10 sections

Indications and uses

Temporary relief of minor aches and pains of muscles and joints due to simple backache arthritic strains bruises sprains

Dosage and administration

Adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 6 years of age: Do not use, consult a doctor.

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Ammonia 2.3%

Camphor 3.1%

Menthol 6.0%

Purpose

OTC - PURPOSE SECTION

External Analgesic

External Analgesic

External Analgesic

Uses

INDICATIONS & USAGE SECTION

Temporary relief of minor aches and pains of muscles and joints due to

  • simple backache
  • arthritic
  • strains
  • bruises
  • sprains

Warnings

WARNINGS SECTION

For external use only

Flammable keep away from fire or flame

Do not use on

OTC - DO NOT USE SECTION

  • wounds
  • damaged skin

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes and mouth
  • do not bandage tightly

Stop use and ask a doctor if

OTC - STOP USE SECTION

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

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

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

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 6 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 6 years of age: Do not use, consult a doctor.

Other Information

OTHER SAFETY INFORMATION

  • Store at room temperature under 86°F (30°C)
  • Flammable. keep away from fire or flame

Inactive ingredients

INACTIVE INGREDIENT SECTION

Geraniol-denatured Alcohol

Questions and comments

OTC - QUESTIONS SECTION

Call 1-310-661-7260 Mon.-Fri. (2p.m. - 3p.m. PST)

Principal Display Panel - 50 mL Bottle Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 51027-0007-1

KINKAN

PAIN
RELIEVING
LINIMENT

MANUFACTURED BY
KINKANDO CO., LTD.350-2 KODAMACHOKYOEI,
HONJO-SHI, SAITAMA 367-0206,
JAPAN

DISTRIBUTED BY
PMAI21112 Figueroa Street Unit B

Carson, CA 90745

1.7 FL OZ (50mL)

Principal Display Panel - 50 mL Bottle LabelPrincipal Display Panel - 50 mL Bottle Label

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2265634ammonia 2.3 % / camphor 3.1 % / menthol 6 % Topical SolutionPSN9
2265634ammonia 23 MG/ML / camphor 31 MG/ML / menthol 60 MG/ML Topical SolutionSCD9
2265634ammonia 2.3 % / camphor 3.1 % / menthol 6 % Topical SolutionSY9

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130349899000105GTIN-13: 0349899000105
EAN-13: 0349899000105
GTIN-12: 349899000105
UPC-A: 349899000105
GTIN storage (14 digits): 00349899000105		kinkan-51027-0007-updated-02.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51027-0007-1KINKAN1 in 1 BOXLINIMENT19
51027-0007-1KINKAN96 in 1 CARTONLINIMENT969

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
ammoniaACTIVE INGREDIENT5138Q19F1X1
camphor (natural)ACTIVE INGREDIENTN20HL7Q9411
mentholACTIVE INGREDIENTL7T10EIP3A1
ammoniaACTIVE MOIETY5138Q19F1X1
camphor (natural)ACTIVE MOIETYN20HL7Q9411
mentholACTIVE MOIETYL7T10EIP3A1
alcoholINACTIVE INGREDIENT3K9958V90M1

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
51027-000751027-0007-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 matching rows.

Name, UNII, Kind table
NameUNIIKind
AMMONIA5138Q19F1XACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
MENTHOLL7T10EIP3AACTIB
ALCOHOL3K9958V90MIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
82025-06-10full-release2026-06-01 01:02:48

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 · 22 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredientIID ingredientUNIIDosage form / routePotencyMaximum daily exposureMatch
alcoholALCOHOL3K9958V90MSHAMPOO / TOPICAL714 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL / TOPICAL561 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MPOWDER, FOR SOLUTION / TOPICAL40 %w/wExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL, SPRAY / TOPICAL561 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MLOTION / TOPICAL25 %w/wExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MGEL / TOPICAL9971 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSHAMPOO / TOPICAL714 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSWAB / TOPICAL2250 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MLOTION / TOPICAL25 %w/wExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MAEROSOL, FOAM / TOPICAL4504 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSPRAY / TOPICAL3633 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MPOWDER, FOR SOLUTION / TOPICAL40 %w/wExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MGEL, METERED / TOPICAL541 mgExact identifier — unii+route
22 equally ranked IID candidates
alcoholALCOHOL3K9958V90MSOLUTION / TOPICAL2445 mgExact identifier — unii+route
22 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
KINKANAMMONIA, CAMPHOR (NATURAL), MENTHOLKINKANDO CO., LTD .f2c0f3e1-792b-4798-bf6d-acd1bbefa2612025-10-21WarningsExact identifier
ndc (package): 51027-0007-1
ndc (product): 51027-0007
ndc11 (package): 51027000701
spl id: 41ac4d77-7e0e-4204-e063-6394a90a3598
spl set id: f2c0f3e1-792b-4798-bf6d-acd1bbefa261

Reported adverse events (FAERS/openFDA)#

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