FERRUM PHOS- ferrum phosphoricum liquid 
Energique, Inc.

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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Drug Facts

ACTIVE INGREDIENTS

Ferrum Phosphoricum 30C

INDICATIONS

To be used according to standard homeopathic indications.

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

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.

DIRECTIONS

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.

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.

INDICATIONS AND USAGE

To be used according to standard homeopathic indications.

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

QUESTIONS

Dist. by Energique, Inc.

201 Apple Blvd

Woodbine, IA 51579

800-869-8078

ENERGIQUE

since 1987

HOMEOPATHIC REMEDY

FERRUM PHOS

30C

1 fl oz (30 ml)

Ferrum Phos 30C

Ferrum Phos 30C

FERRUM PHOS 
ferrum phosphoricum liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0042
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
FERRUM PHOSPHORICUM (UNII: 91GQH8I5F7) (FERROSOFERRIC PHOSPHATE - UNII:91GQH8I5F7) FERRUM PHOSPHORICUM30 [hp_C]  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:44911-0042-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product10/02/2012
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
unapproved homeopathic10/02/2012
Labeler - Energique, Inc. (789886132)
Registrant - Apotheca Company (844330915)
Establishment
NameAddressID/FEIBusiness Operations
Apotheca Company844330915manufacture(44911-0042) , api manufacture(44911-0042) , label(44911-0042) , pack(44911-0042)

Revised: 6/2020
Document Id: 02669d53-7262-4f46-af13-7fd6651d908d
Set id: f013a28c-4461-47a9-a230-01887bbf0a7f
Version: 2
Effective Time: 20200626
 
Energique, Inc.