KINKAN COOL- diphenhydramine hydrochloride, menthol liniment 
KINKANDO CO., LTD .

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Drug Facts

Active ingredients

Diphenhydramine Hydrochloride 2%

Menthol 1%

Purpose

Antihistamine

External Analgesic

Uses

Temporary relief of itching associate with insect bite

Warnings

For external use only

Flammable keep away from fire or flame

Do not use on

  • wounds
  • damaged skin

When using this product

  • avoid contact with the eyes and mouth

Stop use and ask a doctor if

  • 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.

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

Directions

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

Inactive ingredients

Glycerin
Geraniol-denatured Alcohol

Questions and comments

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

Principal Display Panel - 50 mL Bottle Label

NDC 51027-0330-2

KINKAN
COOL
Liniment

EXTERNAL
ANTIPRURITIC
LINIMENT

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

DISTRIBUTED BY
PMAI
1700 W. WALNUT PARKWAY,
COMPTON, CA 90220

1.7 FL OZ (50mL)

Principal Display Panel - 50 mL Bottle Label
KINKAN COOL 
diphenhydramine hydrochloride, menthol liniment
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:51027-0330
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
DIPHENHYDRAMINE HYDROCHLORIDE (UNII: TC2D6JAD40) (DIPHENHYDRAMINE - UNII:8GTS82S83M) DIPHENHYDRAMINE HYDROCHLORIDE1 g  in 50 mL
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.5 g  in 50 mL
Inactive Ingredients
Ingredient NameStrength
GLYCERIN (UNII: PDC6A3C0OX)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:51027-0330-296 in 1 CARTON04/26/2000
11 in 1 BOX
150 mL in 1 BOTTLE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34804/26/2000
Labeler - KINKANDO CO., LTD . (694329470)
Establishment
NameAddressID/FEIBusiness Operations
KINKANDO CO., LTD .715451980manufacture(51027-0330)

Revised: 12/2022
Document Id: f105bb7f-3ec9-0d70-e053-2a95a90a9188
Set id: 82011efe-825c-4102-b6f1-59eff4c8040a
Version: 6
Effective Time: 20221230
 
KINKANDO CO., LTD .