Emvita 7: Package Insert and Label Information

EMVITA 7- lachesis muta venom, lycopodium clavatum spore, anacardium occidentale fruit, phosphorus and sus scrofa adrenal gland liquid
RUBIMED AG

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.

Homeopathic Combination Medicine Indications: Defiance

Ingredients

Lachesis mutus 800 C
Lycopodium 16 LM
Anacard occ. 18 LM
Phosphorus 2l x
Glandula supra. suis 21 x
Alcohol 38 % v/v

TAMPER-EVIDENT

Do not use this product if seal at base of cap is missing or broken.

Direction

12 drops two times per day or as directed by the practitioner.

Warnings

As with any drug, if you are pregnant or nursing a baby, seek the advice of a health professional before using the product.

Keep out of Reach of Children!

PRINCIPAL DISPLAY PANEL — 50 ml Bottle Label

Emvita 7

Homeopathic Combination
Medicine Indications:
Defiance

RUBIMED ®

1.7 Fl.oz. (50ml)

PRINCIPAL DISPLAY PANEL -- 50 ml Bottle Label
(click image for full-size original)
EMVITA 7
lachesis muta venom, lycopodium clavatum spore, anacardium occidentale fruit, phosphorus, and sus scrofa adrenal gland liquid
Product Information
Product Type HUMAN OTC DRUG Item Code (Source) NDC:66343-019
Route of Administration ORAL DEA Schedule
Active Ingredient/Active Moiety
Ingredient Name Basis of Strength Strength
Lachesis Muta Venom (Lachesis Muta Venom) Lachesis Muta Venom 800 [hp_C] in 1 mL
Lycopodium Clavatum Spore (Lycopodium Clavatum Spore) Lycopodium Clavatum Spore 16 [hp_M] in 1 mL
Anacardium Occidentale Fruit (Anacardium Occidentale Fruit) Anacardium Occidentale Fruit 18 [hp_M] in 1 mL
Phosphorus (Phosphorus) Phosphorus 21 [hp_X] in 1 mL
Sus Scrofa Adrenal Gland (Sus Scrofa Adrenal Gland) Sus Scrofa Adrenal Gland 21 [hp_X] in 1 mL
Inactive Ingredients
Ingredient Name Strength
Alcohol 0.38 mL in 1 mL
Packaging
# Item Code Package Description Multilevel Packaging
1 NDC:66343-019-50 50 mL in 1 BOTTLE, DROPPER None
Marketing Information
Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
UNAPPROVED HOMEOPATHIC 05/07/2015
Labeler — RUBIMED AG (480582035)
Establishment
Name Address ID/FEI Operations
RUBIMED AG 480582035 MANUFACTURE (66343-019)
Establishment
Name Address ID/FEI Operations
Omida AG 483268348 MANUFACTURE (66343-019)

Revised: 07/2015 RUBIMED AG

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