COBRAZOL- arnica montana, capsicum annum, crotalus horridus, lachesis muta, naja tripudians gel

CobraZol by

Drug Labeling and Warnings

CobraZol by is a Homeopathic medication manufactured, distributed, or labeled by Nature's Innovation, Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Active Ingredients

Arnica montana (Moutain arnica) 1X HPUS

Capsicum annum (Cayenne pepper) 2X HPUS

Crotalus horridus (Rattlesnake venom) 6X HPUS

Lachesis muta (Bushmaster venom) 8X HPUS

Naja tripudians (Indian Cobra venom) 5X HPUS

The letters HPUS indicate the component(s) in this product is (are) officially monographed in the Homeopathic Pharmacopeia of the United States.

PURPOSE

Purpose

Nerve Injury, Spasms and Muscular Pain

Aching Muscle Symptom Relief

Analgesic

Analgesic

Analgesic

INDICATIONS & USAGE

UsesSymptomatic relief of muscle, joint neuralgia and arthritis pain and stiffness.

WARNINGS

Warnings

For External Use Only.

• If symptoms persist or worsen, discontinue use and seek medical attention.

• This product contains Capsicum, avoid contact with eyes.  If product gets into eyes, flushy with water.  Seek medical attention.

• Do not use on open wounds.

• Pregnant or nursing women and children should not use this product unless advised by a physician.

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

KEEP OUT OF REACH OF CHILDREN

• Keep out of the reach of children.

DOSAGE & ADMINISTRATION

Directions

• Roll gel directly onto affected area.
• Rub thoroughly into area with pain.
• Wash hands immediately to prevent numbing effect and contact with capsicum in eyes.
• Use 3-4 times per day for 1st week.  Use as needed thereafter to relieve discomfort.
• Allow several days for maximum effect.

OTHER SAFETY INFORMATION

Other Information

• Do not use if safety band is broken.
• Intended for use in cases of recurring pain.
• This product is NOT intended to treat disease.  It assists in providing temporary relief.
• This product is for temporary relief of mild to moderate chronic pain.

INACTIVE INGREDIENT

Inactive Ingredients

Benzalkonium Chloride, Boswellia Serrata Resin Extract (Indian Franckincense), Curcuma Longa Root Extract (Curcumin), Glucono Delta Lactone, Isopropyl Alcohol, Menthyl Lactate, Methylcellulose, MSM (Methylsulfonylmethane), Oleic Acid, Propylene Glycol, Purified Water

QUESTIONS

Questions?  Call 866-371-2499

www.cobrazol.xom

Manufactured by: Nature's Innovation, Inc.

5317 Palmero Ct., Buford, GA 30518

PRINCIPAL DISPLAY PANEL

for Chronic Pain Relief

CobraZol

Roll-on Topical Gel

HOMEOPATHIC

• Scent Free
• Analgesic*
• Anti-inflammatory*
• Neuralgia*
• Arthritis Pain*
• Muscle & Joint Pain*

Patent Pending

Net Wt. 3.0 oz. (88.721 mL)

INGREDIENTS AND APPEARANCE

COBRAZOL 
arnica montana, capsicum annum, crotalus horridus, lachesis muta, naja tripudians gel

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 10893-900
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
ARNICA MONTANA (UNII: O80TY208ZW) (ARNICA MONTANA - UNII:O80TY208ZW)	ARNICA MONTANA	1 [hp_X]  in 88.721 mL
CAPSICUM (UNII: 00UK7646FG) (CAPSICUM - UNII:00UK7646FG)	CAPSICUM	2 [hp_X]  in 88.721 mL
CROTALUS HORRIDUS HORRIDUS VENOM (UNII: YHA2XLJ956) (CROTALUS HORRIDUS HORRIDUS VENOM - UNII:YHA2XLJ956)	CROTALUS HORRIDUS HORRIDUS VENOM	6 [hp_X]  in 88.721 mL
LACHESIS MUTA VENOM (UNII: VSW71SS07I) (LACHESIS MUTA VENOM - UNII:VSW71SS07I)	LACHESIS MUTA VENOM	8 [hp_X]  in 88.721 mL
NAJA NAJA VENOM (UNII: ZZ4AG7L7VM) (NAJA NAJA VENOM - UNII:ZZ4AG7L7VM)	NAJA NAJA VENOM	5 [hp_X]  in 88.721 mL

Inactive Ingredients
Ingredient Name	Strength
BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)
TURMERIC (UNII: 856YO1Z64F)
GLUCONOLACTONE (UNII: WQ29KQ9POT)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
METHYL LACTATE, L- (UNII: 0379G9C44S)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
OLEIC ACID (UNII: 2UMI9U37CP)
PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
WATER (UNII: 059QF0KO0R)
METHYLCELLULOSE (1500 CPS) (UNII: P0NTE48364)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 10893-900-03	1 in 1 PACKAGE	08/21/2013
1		88.721 mL in 1 BOTTLE, DISPENSING; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/21/2013

Labeler - Nature's Innovation, Inc. (602969854)

Establishment
Name	Address	ID/FEI	Business Operations
Nature's Innovation, Inc.		602969854	manufacture(10893-900)