OTC Medication Information: Weh-Weh Pain Reliever Gel

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

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
(click image for full-size original)

WEH-WEH PAIN RELIEVER GEL
menthol gel
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:35192-020
Route of Administration TOPICAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
MENTHOL (MENTHOL) MENTHOL 6 g in 120 g
Inactive Ingredients
Ingredient Name Strength
EUCALYPTUS OIL
CHAMAEMELUM NOBILE FLOWER
FD&C RED NO. 3
POTASSIUM SORBATE
SALIX ALBA BARK
HORSE CHESTNUT
ARNICA MONTANA
BROMELAINS
BUTYLENE GLYCOL
CAPSICUM
TILIA CORDATA FLOWER
GLUCOSAMINE SULFATE
MELISSA OFFICINALIS
DIMETHYL SULFONE
AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER
HARPAGOPHYTUM PROCUMBENS ROOT
POLYSORBATE 60
WATER
ROSEMARY
EDETIC ACID
ALCOHOL
XANTHAN GUM
ALOE VERA LEAF
Product Characteristics
Color green Score
Shape Size
Flavor MENTHOL Imprint Code
Contains
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:35192-020-02 120 g in 1 TUBE None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
OTC Monograph Drug M017 01/31/2016
Labeler — CA-BOTANA INTERNATIONAL (106276728)
Establishment
Name Address ID/FEI Operations
CA-BOTANA INTERNATIONAL 106276728 manufacture (35192-020)

Revised: 10/2023 CA-BOTANA INTERNATIONAL

Our database comes directly from the FDA’s central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA’s repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

Our database comes directly from the FDA's central repository of drug labels and package inserts under the Structured Product Labeling standard. OTCLabels.com provides the full over the counter products subset of the FDA's repository. Medication information provided here is not intended as a substitute for direct consultation with a qualified health professional.

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