FDA.reportPublic FDA data

Attention Deficit Severe Drops

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC
Effective date
2026-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
monthly-update
Hydrated at
2026-06-03 17:49:33

Label at a glance#

ProductAttention Deficit Severe Drops 2147
Active ingredient.GAMMA.-AMINOBUTYRIC ACID, GINKGO, BOS TAURUS BRAIN, BOS TAURUS HYPOTHALAMUS, BEEF KIDNEY, BEEF LIVER, BOS TAURUS PANCREAS, SUS SCROFA PINEAL GLAND, SILVER NITRATE, COFFEA ARABICA SEED, ROASTED, LYCOPODIUM CLAVATUM SPORE, AMARYLLIS BELLADONNA WHOLE, PHOSPHORUS, AMBERGRIS, BARIUM CARBONATE, BARIUM CHLORIDE DIHYDRATE, BUFO BUFO CUTANEOUS GLAND, HYOSCYAMUS NIGER, GONORRHEAL URETHRAL SECRETION HUMAN, DATURA STRAMONIUM, LYCOSA TARANTULA, THUJA OCCIDENTALIS LEAF, BOVINE TUBERCULIN, VERATRUM ALBUM ROOT, INSULIN GLULISINE
Label structure9 sections

Dosage and administration

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

GABA 3X
Ginkgo biloba 3X
Brain 6X
Hypothalamus 6X
Kidney 6X
Liver 6X
Pancreas 6X
Pineal 6X
Argentum nitricum 30X
Coffea tosta 30X
Lycopodium clavatum 30X
Belladonna 60X
Phosphorus 60X
Ambra grisea 60X, 100X
Baryta carbonica 60X, 100X
Baryta muriatica 60X, 100X
Bufo rana 60X, 100X
Hyoscyamus niger 60X, 100X
Medorrhinum 60X, 100X
Stramonium 60X, 100X
Tarentula hispana 60X, 100X
Thuja occidentalis 60X, 100X
Tuberculinum 60X, 100X
Veratrum album 60X, 100X
DNA insulin 60X, 100X, 200X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of moderate or more severe excitability, fidgeting, or lack of restraint or focus.*

OTC - PURPOSE SECTION

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

WARNINGS

WARNINGS SECTION

In case of overdose, get medical help or contact a poison control center right away.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

OTC - PREGNANCY OR BREAST FEEDING SECTION

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 drops up to 3 times per day. Consult a physician for use in children under 12 years of age.

OTHER INFORMATION

OTHER SAFETY INFORMATION

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

10% ethanol, purified water, 8% vegetable glycerin (from soy).

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Attention Deficit Severe Drops

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2147-22026-01-09C16284748780-11030e365-062f-111a-e063-dadaa90a10e2C147
63083-2147-22026-01-09C16284748780-11030e365-062f-111a-e063-dadaa90a10e2C147
63083-2147-22024-01-30C16284748780-11030e365-062f-111a-e063-dadaa90a10e2C147
63083-2147-22024-01-30C16284748780-11030e365-062f-111a-e063-dadaa90a10e2C147

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2147-2Attention Deficit Severe Drops214759 mL in 1 BOTTLE, DROPPERLIQUID592

Products#

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

DailyMed product names page 1 of 1 · 31 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-214763083-2147-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 27 matching rows.

Name, UNII, Kind table
NameUNIIKind
.GAMMA.-AMINOBUTYRIC ACID2ACZ6IPC6IACTIB
GINKGO19FUJ2C58TACTIB
BOS TAURUS BRAINA1YEE2DB8ZACTIB
BOS TAURUS HYPOTHALAMUSS6G2NLH4Y7ACTIB
BEEF KIDNEY5HOC10FSICACTIB
BEEF LIVERW8N8R55022ACTIB
BOS TAURUS PANCREAS1M529TNT1DACTIB
SUS SCROFA PINEAL GLAND050QZ2EDK7ACTIB
SILVER NITRATE95IT3W8JZEACTIB
COFFEA ARABICA SEED, ROASTED9H58JRT35EACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
AMARYLLIS BELLADONNA WHOLE11B89M58UNACTIB
PHOSPHORUS27YLU75U4WACTIB
AMBERGRISXTC0D02P6CACTIB
BARIUM CARBONATE6P669D8HQ8ACTIB
BARIUM CHLORIDE DIHYDRATEEL5GJ3U77EACTIB
BUFO BUFO CUTANEOUS GLANDQ59QU6N72QACTIB
HYOSCYAMUS NIGER4WRK2153H3ACTIB
GONORRHEAL URETHRAL SECRETION HUMAN9BZG9E3I8FACTIB
DATURA STRAMONIUMG6W4F0V8Z3ACTIB
LYCOSA TARANTULA86M454L2TTACTIB
THUJA OCCIDENTALIS LEAF0T0DQN8786ACTIB
BOVINE TUBERCULINHKD62G79N5ACTIB
VERATRUM ALBUM ROOTQNS6W5US1ZACTIB
INSULIN GLULISINE7XIY785AZDACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:16:25

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
Attention Deficit Severe Drops 2147ATTENTION DEFICIT SEVERE DROPSProfessional Complementary Health Formulascd45062c-f3b1-439f-a559-3582d5c621732026-01-08WarningsExact identifier
ndc (package): 63083-2147-2
ndc (product): 63083-2147
ndc11 (package): 63083214702
spl id: 964caa36-9f97-451e-bbc2-b425492baa15
spl set id: cd45062c-f3b1-439f-a559-3582d5c62173

Reported adverse events (FAERS/openFDA)#

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