WEH-WEH PAIN RELIEVER GEL- menthol gel 
CA-BOTANA INTERNATIONAL

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Weh-Weh Pain Relief Gel

OTC - ACTIVE INGREDIENT

Menthol 5% Topical Analgesic

Other Safety Information

Protect this product from excessive heat and direct sun

OTC - ASK DOCTOR

Stop use and ask a doctor if redness is present.irritation develops. conditions worsens or symtoms persist more than 7 days. symtoms clear up and occur again within a few days

OTC - PURPOSE SECTION

Uses: for temporary relief of minor aches and pains of muscles and joints associated with. simple aches. back aches. arthritis.strains.bruises.sprains.

Keep out of reach of children

Keep out of reach of children

INACTIVE INGREDIENTS

Aesculus hippocastanum (Horse Chestnut), Aloe barbadensis miller, Aloe barbadensis miller (Aloe Vera), Amonium Acrylcydimethyltaurate/VPCcopolymer, Arnica montana (Arnica), Bromelain, Butylene Glycol, Capsicum annum (Capsicum), Chamaemelum nobile (Chamomile), Ethyl alcohol, Eucalyptus globules (Eucaliptus) oil, FD&C Green # 3, Glucosamine Sulfate, Harpagophytum procumbens (Devil’s Claw), Melissa officinalis (Lemon Balm), Methyl Sulfonyl Methane (MSM), Polysorbate-60, Potassium Sorbate, Purified Water, Rosmarinus officinalis (Rosemary), Salix alba (Willow Bark), Edetic Acid, Tilia cordata (Linden), Xanthan Gum

Warnings

Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away

Dosage & Admnistration

External topical analgesic Topical massage gel no more than 4 times daily

Indications & usage

Apply generous amount of gel directly affected area massage into painful area until thoroughly absorbed into skin

Package label princip[al panel

 https://direct.fda.gov/apex/apex_util.get_blob_file?a=100&s=14075775173179&p=114&d=53000640981392638&i=53003644846473016&p_pk1=18134&p_pk2=865-Weh-Weh-Gel.jpg&p_ck=DD4DEEF6923E319E9AB8559D94E333E3

WEH-WEH PAIN RELIEVER GEL 
menthol gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:35192-020
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL6 g  in 120 g
Inactive Ingredients
Ingredient NameStrength
EUCALYPTUS OIL (UNII: 2R04ONI662)  
CHAMAEMELUM NOBILE FLOWER (UNII: O2T154T6OG)  
FD&C RED NO. 3 (UNII: PN2ZH5LOQY)  
POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
SALIX ALBA BARK (UNII: 205MXS71H7)  
HORSE CHESTNUT (UNII: 3C18L6RJAZ)  
ARNICA MONTANA (UNII: O80TY208ZW)  
BROMELAINS (UNII: U182GP2CF3)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
CAPSICUM (UNII: 00UK7646FG)  
TILIA CORDATA FLOWER (UNII: CFN6G1F6YK)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
MELISSA OFFICINALIS (UNII: YF70189L0N)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
HARPAGOPHYTUM PROCUMBENS ROOT (UNII: 1OYM338E89)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
WATER (UNII: 059QF0KO0R)  
ROSEMARY (UNII: IJ67X351P9)  
EDETIC ACID (UNII: 9G34HU7RV0)  
ALCOHOL (UNII: 3K9958V90M)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ALOE VERA LEAF (UNII: ZY81Z83H0X)  
Product Characteristics
ColorgreenScore    
ShapeSize
FlavorMENTHOLImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:35192-020-02120 g in 1 TUBE; Type 0: Not a Combination Product01/31/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/31/2016
Labeler - CA-BOTANA INTERNATIONAL (106276728)
Establishment
NameAddressID/FEIBusiness Operations
CA-BOTANA INTERNATIONAL106276728manufacture(35192-020)

Revised: 10/2023
Document Id: 079ac9a2-8a00-2910-e063-6394a90ad858
Set id: 25606ff8-8775-2d41-e054-00144ff88e88
Version: 21
Effective Time: 20231013
 
CA-BOTANA INTERNATIONAL