FDA.reportPublic FDA data

E07

Manufacturer
Apex Energetics Inc.
Effective date
2024-01-09
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:25:19

Label at a glance#

ProductE07 TYPE A BALANCE
Active ingredientSTRYCHNOS IGNATII SEED, LYCOPUS VIRGINICUS, PASSIFLORA INCARNATA TOP, SCUTELLARIA LATERIFLORA WHOLE, CRATAEGUS LAEVIGATA FRUIT, COLCHICUM AUTUMNALE BULB, ARABICA COFFEE BEAN, QUININE ARSENITE, AMERICAN GINSENG, ACONITUM NAPELLUS, STRYCHNOS NUX-VOMICA SEED, THYROID, UNSPECIFIED, STRYCHNINE PHOSPHATE DIHYDRATE, VISCUM ALBUM FRUITING TOP, GELSEMIUM SEMPERVIRENS ROOT, ECHINACEA PURPUREA, ESCHSCHOLZIA CALIFORNICA, HOPS
Label structure7 sections

Dosage and administration

Adults & children ages 12 years and over: Take 10 drops under the tongue in the morning and evening, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients

Aconitum napellus

4X 6X 8X

Aralia quinquefolia

9X 12X 15X

Chininum arsenicosum

6X

Coffea cruda

6X 8X 10X 12X

Colchicum autumnale

6X 12X

Crataegus oxyacantha fruit

4X

Echinacea purpurea

3X

Eschscholtzia californica

1X

Gelsemium sempervirens

6X 9X 12X

Humulus lupulus

1X

Ignatia amara

4X 6X 8X

Lycopus virginicus

1X

Nux vomica

7X 9X 12X

Passiflora incarnata

1X

Scutellaria lateriflora

1X

Strychninum phosphoricum

6X 12X

Thyroidinum

7C 9C

Viscum album fruiting top

3X

INDICATIONS & USAGE SECTION

Uses:

OTC - PURPOSE SECTION

For temporary relief of minor:

occasional sleeplessness*

menstrual cramping*
restlessness*

irritability*

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

WARNINGS SECTION

OTC - PREGNANCY OR BREAST FEEDING SECTION

If pregnant or breastfeeding, ask a health professional before use.

OTHER SAFETY INFORMATION

Do not use if clear seal over the cap is broken or missing.

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.

OTC - STOP USE SECTION

Stop use and ask a doctor if occasional sleeplessness, menstrual cramping, restlessness, irritability, or other symptoms do not improve within 7 days or are accompanied by fever.

Directions:

DOSAGE & ADMINISTRATION SECTION

Adults & children ages 12 years and over: Take 10 drops under the tongue in the morning and evening, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients

INACTIVE INGREDIENT SECTION

alcohol (20% by volume), distilled water

OTC - QUESTIONS SECTION

Distributed by Apex Energetics. Questions?

16592 Hale Ave., Irvine, CA 92606, USA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

FUTUREPLEX® E07

ANTITOX®

TYPE-A BALANCE™

Homeopathic Formula

Occasional Sleeplessness*

Restlessness*

1 fl oz (30 mL)

Alcohol 20% by Volume

E0723-0921E0723-0921

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
3c386306-c48a-413e-bb69-70cb268496f3Product name120210727
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810
22bca8fc-c2b1-897d-b515-117a7522ccaeProduct name320150731

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63479-0507-1E07TYPE A BALANCE30 mL in 1 BOTTLE, GLASSSOLUTION/ DROPS302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63479-0507E07 TYPE A BALANCE (ACONITUM NAPELLUS, ARALIA QUINQUEFOLIA, CHININUM ARSENICOSUM, COFFEA CRUDA, COLCHICUM AUTUMNALE, CRATAEGUS OXYACANTHA FRUIT, ECHINACEA PURPUREA, ESCHSCHOLTZIA CALIFORNICA, HUMULUS LUPULUS, IGNATIA AMARA, LYCOPUS VIRGINICUS, NUX VOMICA, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, STRYCHNINUM PHOSPHORICUM, THYROIDINUM, VISCUM ALBUM FRUITING TOP, YELLOW JASMINE ROOT) SOLUTION/ DROPS [APEX ENERGETICS INC.]2Current NDC, 1 package rows20240110_06c113f5-63be-f431-e063-6294a90a7d4f.zip

Products#

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

DailyMed product names page 1 of 1 · 25 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63479-050763479-0507-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
NameUNIIKind
STRYCHNOS IGNATII SEED1NM3M2487KACTIB
LYCOPUS VIRGINICUSTWH5125Q6FACTIB
PASSIFLORA INCARNATA TOPCLF5YFS11OACTIB
SCUTELLARIA LATERIFLORA WHOLE7BP4DH5PDCACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT
CRATAEGUS LAEVIGATA FRUITD5RZ7MF1YFACTIB
COLCHICUM AUTUMNALE BULB993QHL78E6ACTIB
ARABICA COFFEE BEAN3SW678MX72ACTIB
QUININE ARSENITE42QO5P0NLMACTIB
AMERICAN GINSENG8W75VCV53QACTIB
ACONITUM NAPELLUSU0NQ8555JDACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
THYROID, UNSPECIFIED0B4FDL9I6PACTIB
STRYCHNINE PHOSPHATE DIHYDRATETD67SYY51DACTIB
VISCUM ALBUM FRUITING TOPBK9092J5MPACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
ECHINACEA PURPUREAQI7G114Y98ACTIB
ESCHSCHOLZIA CALIFORNICA9315HN272XACTIB
HOPS01G73H6H83ACTIB

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
E07 TYPE A BALANCEACONITUM NAPELLUS, ARALIA QUINQUEFOLIA, CHININUM ARSENICOSUM, COFFEA CRUDA, COLCHICUM AUTUMNALE, CRATAEGUS OXYACANTHA FRUIT, ECHINACEA PURPUREA, ESCHSCHOLTZIA CALIFORNICA, HUMULUS LUPULUS, IGNATIA AMARA, LYCOPUS VIRGINICUS, NUX VOMICA, PASSIFLORA INCARNATA, SCUTELLARIA LATERIFLORA, STRYCHNINUM PHOSPHORICUM, THYROIDINUM, VISCUM ALBUM FRUITING TOP, YELLOW JASMINE ROOTApex Energetics Inc.06c113f5-63be-f431-e063-6294a90a7d4f2024-01-09WarningsExact identifier
ndc (package): 63479-0507-1
ndc (product): 63479-0507
ndc11 (package): 63479050701
spl id: 0e892003-98dd-bbc6-e063-6294a90a5233
spl set id: 06c113f5-63be-f431-e063-6294a90a7d4f

Reported adverse events (FAERS/openFDA)#

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