BAROX- menthol gel 
KTAIGA 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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Active ingredient

Active ingredient: Menthol 2.5%

Inactive ingredient

Inactive ingredients:
Water, Alcohol, Propylene Glycol, Germanium Dioxide, Allantoin, Carbomer, Triethanolamine, PEG-60 Hydrogenated Castor Oil, Disodium EDTA, Methylparaben

Purpose

Purpose: Topical Analgesic

Warnings

Warnings: For external use only

Keep out of reach of children

Keep out of reach of children:
Keep out of reach of children to avoid accidental ingestion.
If swallowed, get medical help or contact a Poison Control Center immediately.

Uses

Uses:
Temporarily relieves the minor pains of muscles and joints associated with:
simple backache and arthritis

Dosage and administration

Dosage and administration:
adults and children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
children under 12 years of age: ask a doctor

Description

Ask a doctor before use if you have redness over the affected area.

Do not use: on wounds or damaged skin

Stop use and ask a doctor if excessive skin irritation occurs.

Other information:
Store in a cool dry place with lid closed tightly

Question
Contact: smyou2@nate.com

PACKAGE LABEL. PRINCIPAL DISPLAY PANEL

Image of carton

BAROX 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52227-100
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL3 g  in 120 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R) 82.2 g  in 120 mL
ALCOHOL (UNII: 3K9958V90M) 18 g  in 120 mL
PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 4.8 g  in 120 mL
GERMANIUM DIOXIDE (UNII: 5O6CM4W76A) 0.96 g  in 120 mL
TROLAMINE (UNII: 9O3K93S3TK) 0.6 g  in 120 mL
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:52227-100-01120 mL in 1 CARTON
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart34803/01/2012
Labeler - KTAIGA CO., LTD. (557819324)
Registrant - KTAIGA CO., LTD. (557819324)
Establishment
NameAddressID/FEIBusiness Operations
KTAIGA CO., LTD.557819324manufacture(52227-100)

Revised: 8/2012
Document Id: 32f8722a-d964-4d1d-9be8-b62c686f83f0
Set id: 8973fd30-1fb5-4d00-bed3-393f0689de6e
Version: 4
Effective Time: 20120815
 
KTAIGA CO., LTD.