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Manufacturer
Engergique, Inc. | Apotheca Company
Effective date
2024-11-05
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-01 20:50:25

Label at a glance#

ProductADD HP
Active ingredient.GAMMA.-AMINOBUTYRIC ACID, LEVODOPA, NOREPINEPHRINE BITARTRATE, SEROTONIN HYDROCHLORIDE, CORTICOTROPIN, ANACARDIUM OCCIDENTALE FRUIT, ARSENIC TRIOXIDE, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, TRIBASIC CALCIUM PHOSPHATE, HYOSCYAMUS NIGER, LYCOPODIUM CLAVATUM SPORE, DATURA STRAMONIUM
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 1 to 2 times 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): 4.53% of Adrenocorticotrophin 8X, 12X, 30X, 12C, 30C, Anacardium Orientale 30C, Arsenicum Album 30C, Baryta Carbonica 30C, Calcarea Carbonica 30C, Calcarea Phosphorica 30C, Hyoscyamus Niger 30C, Lycopodium Clavatum 30C, Norepinephrine (Bitartrate) 12X, 30C, 12C, 30C, Serotonin (Hydrochloride) 12C, 30C, Stramonium 30C; 2.27% of GABA (Gamma-Aminobutyric Acid) 12C, 30C, L-Dopa 12C, 30C; 1.51% of GABA (Gamma-Aminobutyric Acid) 6X, 12X, 30X; 0.10% of Norepinephrine (Bitartrate) 6X; .0.3% of L-Dopa 6X, 12X, 30X, Serotonin (Hydrochloride) 6X, 12X, 30X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve symptoms associated with attention disorders, such as lack of attention, poor concentration, hyperactivity, procrastination, and memory and comprehension problems.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breast-feeding, ask a health care 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 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 to 2 times 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 associated with attention disorders, such as lack of attention, poor concentration, hyperactivity, procrastination, and memory and comprehension problems.**

**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

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1 fl. oz. (30 ml)

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FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0493-12024-11-05C16284748780-1ba0f9c33-1110-a910-e053-dadaa90a0b85Drug Facts:
44911-0493-12021-01-29C16284748780-1ba0f9c33-1110-a910-e053-dadaa90a0b85Drug Facts:

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-049344911-0493-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 15 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
d3e99cca-0892-4399-9e59-dc1da8f1fbb390db5fa1-9e75-42d1-8fab-d5ae4b018c702024-11-05WarningsExact identifier
spl id: d3e99cca-0892-4399-9e59-dc1da8f1fbb3
spl set id: 90db5fa1-9e75-42d1-8fab-d5ae4b018c70

Reported adverse events (FAERS/openFDA)#

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