HFM CORD- coxsackie nosode a3, a4, a5, a7, b1, b3, b5 liquid

HFM CORD by

Drug Labeling and Warnings

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

Drug Details [pdf]

ACTIVE INGREDIENTS:

(in each drop): 14.19% of Coxsackie Nosode A3, A4, A5, A7, B1, B3, B5, 30C. 0.10% of Coxsackie Nosode A5 12C; Coxsackie Nosode A3, A4, A7, B1, B3, B5, 6C.

INDICATIONS:

May temporarily relieve symptoms such as headaches.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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.

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:

Adults and children 5 to 10 drops orally, 1 time daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

INDICATIONS:

May temporarily relieve symptoms such as headaches.**

**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

INACTIVE INGREDIENTS:

Demineralized water, 20% Ethanol.

QUESTIONS:

Dist. by Energique, Inc.
201 Apple Blvd
Woodbine, IA 51579 800-869-8078

PACKAGE LABEL DISPLAY:

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

HFM CORD

1 fl. oz. (30 ml)

INGREDIENTS AND APPEARANCE

HFM CORD 
coxsackie nosode a3, a4, a5, a7, b1, b3, b5 liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44911-0601
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
HUMAN COXSACKIEVIRUS A (UNII: 6F61V9UVRC) (HUMAN COXSACKIEVIRUS A - UNII:6F61V9UVRC)	HUMAN COXSACKIEVIRUS A	6 [hp_C]  in 1 mL
HUMAN COXSACKIEVIRUS A7 (UNII: P3026TK92O) (HUMAN COXSACKIEVIRUS A7 - UNII:P3026TK92O)	HUMAN COXSACKIEVIRUS A7	6 [hp_C]  in 1 mL
HUMAN COXSACKIEVIRUS B (UNII: NCM5G1A67U) (HUMAN COXSACKIEVIRUS B - UNII:NCM5G1A67U)	HUMAN COXSACKIEVIRUS B	6 [hp_C]  in 1 mL
HUMAN COXSACKIEVIRUS B1 (UNII: ADL68M27WD) (HUMAN COXSACKIEVIRUS B1 - UNII:ADL68M27WD)	HUMAN COXSACKIEVIRUS B1	6 [hp_C]  in 1 mL
HUMAN COXSACKIEVIRUS B3 (UNII: 69O1DAO10G) (HUMAN COXSACKIEVIRUS B3 - UNII:69O1DAO10G)	HUMAN COXSACKIEVIRUS B3	12 [hp_C]  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: 44911-0601-1	30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	05/24/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		05/24/2021

Labeler - Energique, Inc. (789886132)

Registrant - Apotheca Company (844330915)

Establishment
Name	Address	ID/FEI	Business Operations
Apotheca Company		844330915	manufacture(44911-0601) , api manufacture(44911-0601) , label(44911-0601) , pack(44911-0601)