LIBERATE- nux vomica tablet
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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LIBERATE

Nux Vomica 60C 200C 1000C

Nux Vomica 60C 200C 1000C........Alcoholism

Helps to minimize the effects of alcoholism as per Materia Medica.

Stop use and ask doctor if symptoms of alcoholism persist.

Do not use if you have an allergy or hypersensitivity to components of the formula.
Not for Pediatric use.

If pregnant or breast feeding ask a health professional before use.

Keep out of the reach of children.

Adults take 3 tablets every 10 days, beginning with the number 1 strip, then 10 days later the number 2 strip, and 10 days after take the number 3 strip tablets. Dissolve slowly in mouth.

Store in a cool and dry place.

Lactose, Magnesium Stearate, Potato Starch, Talc, Gelatin

P.O. Box 1261, Downey, CA 90240 www.nartexlabs.com

Made in Mexico by:

NARTEX

Laboratories Homeopaticos, S.A. de C.V.

Calz. Lazaro Cardenas 770 Ote.

Col. Eduardo Guerra, C.P. 27280

Torreon, Coah., Mexico

Homeopathic Medicine

Liberate

Nux Vomica

Mexican Tradition

9 Tablets

Relieves syptoms of Alcoholism as per the William Boericke Materia Medica

liberate

LIBERATE
nux vomica tablet

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:34666-004
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919)	STRYCHNOS NUX-VOMICA SEED	50 [hp_X]

Ingredient Name	Strength
Inactive Ingredients
LACTOSE (UNII: J2B2A4N98G)
MAGNESIUM STEARATE (UNII: 70097M6I30)
STARCH, POTATO (UNII: 8I089SAH3T)
TALC (UNII: 7SEV7J4R1U)
GELATIN (UNII: 2G86QN327L)

Product Characteristics
Color	white (white)	Score	no score
Shape	ROUND	Size	10mm
Flavor		Imprint Code	none
Contains

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:34666-004-90	9 in 1 BLISTER PACK; Type 0: Not a Combination Product	08/01/2009	06/20/2013

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		08/01/2009	06/20/2013

Labeler - NARTEX LABORATORIOS HOMEOPATICOS SA DE CV (589914576)

Registrant - NARTEX LABORATORIOS HOMEOPATICOS SA DE CV (589914576)

Name	Address	ID/FEI	Business Operations
Establishment
NARTEX LABORATORIOS HOMEOPATICOS SA DE CV		589914576	manufacture(34666-004)

Revised: 6/2013

Document Id: 6cc3a007-fa56-7e6c-e053-2a91aa0ab251

Set id: 9453f2da-3335-4383-af66-0598ce6af817

Version: 6

Effective Time: 20130620

NARTEX LABORATORIOS HOMEOPATICOS SA DE CV