HFM CORD

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-25
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:28:23

Label at a glance#

ProductHFM CORD
Active ingredientHUMAN COXSACKIEVIRUS A, HUMAN COXSACKIEVIRUS A7, HUMAN COXSACKIEVIRUS B, HUMAN COXSACKIEVIRUS B1, HUMAN COXSACKIEVIRUS B3
Label structure9 sections

Dosage and administration

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.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS:

OTC - ACTIVE INGREDIENT SECTION

(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:

OTC - PURPOSE SECTION

May temporarily relieve symptoms such as headaches.**

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

WARNINGS:

WARNINGS SECTION

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:

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

DIRECTIONS:

DOSAGE & ADMINISTRATION SECTION

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:

INDICATIONS & USAGE SECTION

May temporarily relieve symptoms such as headaches.**

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

INACTIVE INGREDIENTS:

INACTIVE INGREDIENT SECTION

Demineralized water, 20% Ethanol.

QUESTIONS:

OTC - QUESTIONS SECTION

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

PACKAGE LABEL DISPLAY:

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

ENERGIQUE

SINCE 1987

HOMEOPATHIC REMEDY

HFM CORD

1 fl. oz. (30 ml)

HFM CORDHFM CORD

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0601-12024-10-25C16284748780-1f386c64a-1fd3-0266-e053-dadaa90a7c1aDRUG FACTS:
44911-0601-12023-01-30C16284748780-1f386c64a-1fd3-0266-e053-dadaa90a7c1aDRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0601-1HFM CORD30 mL in 1 BOTTLE, DROPPERLIQUID302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0601HFM CORD (COXSACKIE NOSODE A3, A4, A5, A7, B1, B3, B5) LIQUID [ENERGIQUE, INC.]2Current NDC, Legacy NDC, 1 package rows20241027_18a61569-fc0e-4513-a54a-0ea24783744c.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-060144911-0601-1

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 7 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
HFM CORDCOXSACKIE NOSODE A3, A4, A5, A7, B1, B3, B5Energique, Inc.18a61569-fc0e-4513-a54a-0ea24783744c2024-10-25WarningsExact identifier
ndc (package): 44911-0601-1
ndc (product): 44911-0601
ndc11 (package): 44911060101
spl id: 632dc16d-3460-4a92-b544-3cffeb66ab6c
spl set id: 18a61569-fc0e-4513-a54a-0ea24783744c

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.