CATS CLAW- uncaria tomentosa liquid

Cats Claw by

Drug Labeling and Warnings

Cats Claw by is a Homeopathic medication manufactured, distributed, or labeled by Energique, Inc., Apotheca Company. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT:

(in each drop): 33.33% of Uncaria Tomentosa 6X, 12X, 30X.

INDICATIONS:

For relief of symptoms associated with Chronic Fatigue Syndrome, Fibromyalgia and Lyme Disease.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

WARNINGS:

If pregnant or breastfeeding, ask a health professional before use.

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Do not use if tamper evident seal is broken or missing.

Store in a cool, dry place.

KEEP OUT OF REACH OF CHILDREN:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

Take 1 drop under tongue, once daily. Consult a physician for use in children under 12 years of age.

INDICATIONS:

For relief of symptoms associated with Chronic Fatigue Syndrome, Fibromyalgia and Lyme Disease.**

**These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.,

201 Apple Blvd.

Woodbine, IA 51579    800.868.8078

PACKAGE LABEL DISPLAY:

ENERGIQUE
SINCE 1987
HOMEOPATHIC REMEDY
CATS'S CLAW
6X, 12X, 30X
1 fl. oz. (30 ml)

INGREDIENTS AND APPEARANCE

CATS CLAW 
uncaria tomentosa liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44911-0432
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
CAT'S CLAW (UNII: 9060PRM18Q) (CAT'S CLAW - UNII:9060PRM18Q)	CAT'S CLAW	6 [hp_X]  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
WATER (UNII: 059QF0KO0R)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44911-0432-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	02/08/2018

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		02/08/2018

Labeler - Energique, Inc. (789886132)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(44911-0432) , api manufacture(44911-0432) , label(44911-0432) , pack(44911-0432)