FUCUS VESICULOSUS- fucus vesiculosus, liquid
Apotheca Company

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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Fucus Vesiculosus 30C

ACTIVE INGREDIENT: Fucus Vesiculosus 30C.

INDICATIONS: for temporary relief of symptoms of non-toxic goiter and enlarged thyroid in the obese. Supports digestion and reduces flatulence.

WARNINGS: If pregnant or breast-feeding, 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.

INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.

KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

SUGGESTED USE: Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS: For temporary relief of symptoms of non-toxic goiter and enlarged thyroid in the obese. Supports digestion and reduces flatulence.

Dist. by Energique, Inc.

201 Apple Blvd.

Woodbine, IA 51579

800-869-8078

ENERGIQUE

FUCUS VESICULOSUS 30C

1 fl. oz. (30 ml)

Fucus Vesiculosus 30C

FUCUS VESICULOSUS
fucus vesiculosus, liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC:57520-0676
Route of Administration	ORAL

Ingredient Name	Basis of Strength	Strength
Active Ingredient/Active Moiety
FUCUS VESICULOSUS (UNII: 535G2ABX9M) (FUCUS VESICULOSUS - UNII:535G2ABX9M)	FUCUS VESICULOSUS	30 [hp_C] in 1 mL

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

#	Item Code	Package Description	Marketing Start Date	Marketing End Date
Packaging
1	NDC:57520-0676-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	04/11/2011	09/21/2022

Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
Marketing Information
unapproved homeopathic		04/11/2011	09/21/2022

Labeler - Apotheca Company (844330915)

Registrant - Apotheca Company (844330915)

Name	Address	ID/FEI	Business Operations
Establishment
Apotheca Company		844330915	manufacture(57520-0676) , api manufacture(57520-0676) , label(57520-0676) , pack(57520-0676)

Revised: 5/2022

Document Id: 084614ed-3ecc-4225-9b10-53836cdcf8f9

Set id: 9b653dbc-51ef-4121-8743-b349caef548a

Version: 3

Effective Time: 20220523

Apotheca Company