FDA.reportPublic FDA data

Cerebrapar

Manufacturer
Energique, Inc. | Apotheca Company
Effective date
2024-10-24
Label type
HUMAN OTC DRUG LABEL
Version
4
Source
full-release
Hydrated at
2026-06-01 02:28:29

Label at a glance#

ProductCerebrapar
Active ingredientBAPTISIA TINCTORIA ROOT, SUS SCROFA CEREBRUM, CLAVICEPS PURPUREA SCLEROTIUM, BARIUM CARBONATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, GELSEMIUM SEMPERVIRENS ROOT, POTASSIUM PHOSPHATE, DIBASIC, LYCOPODIUM CLAVATUM SPORE, DELPHINIUM STAPHISAGRIA SEED
Label structure9 sections

Dosage and administration

Adults and children 5 to 10 drops orally, 3 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): 14.26% of Baryta Carbonica 12X, Calcarea Carbonica 12X, Cerebrum Suis 6X, Gelsemium Sempervirens 12X, Kali Phosphoricum 12X, Lycopodium Clavatum 12X, Staphysagria 12X; 0.10% of Baptisia Tinctoria 3X, Secale Cornutum 6X.

INDICATIONS:

OTC - PURPOSE SECTION

May temporarily relieve nervous twitch, confusion and forgetfulness.**

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

WARNINGS:

WARNINGS SECTION

If pregnant or breastfeeding, 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, 3 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 nervous twitch, confusion and forgetfulness.**

**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

CEREBRAPAR

1 fl. oz. (30 ml)

CerebraparCerebrapar

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
efd58dcf-540a-4531-8766-e713129ca6f2Product name120250307
4b7700e3-6e0e-45e5-9d22-6f754d61386eProduct name220250304
726062af-1135-4707-a1d7-57256991bbf9Product name220250226
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
19c71a3d-ed9c-166b-a7e5-38c250c35631Product name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
44911-0317-12024-10-24C16284748780-1d6a99b39-5421-a426-e053-dadaa90af4c2DRUG FACTS:
44911-0317-12022-01-28C16284748780-1d6a99b39-5421-a426-e053-dadaa90af4c2DRUG FACTS:

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
44911-0317-1Cerebrapar30 mL in 1 BOTTLE, DROPPERLIQUID304

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
44911-0317CEREBRAPAR (BAPTISIA TINCTORIA, CEREBRUM SUIS, SECALE CORNUTUM, BARYTA CARBONICA, CALCAREA CARBONICA, GELSEMIUM SEMPERVIRENS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, STAPHYSAGRIA) LIQUID [ENERGIQUE, INC.]4Current NDC, Legacy NDC, 1 package rows20241027_cf6b59ee-64dc-4126-ade9-a92b4c7a3af9.zip

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
44911-031744911-0317-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 11 matching rows.

Name, UNII, Kind table
NameUNIIKind
BAPTISIA TINCTORIA ROOT5EF0HWI5WUACTIB
SUS SCROFA CEREBRUM4GB5DQR532ACTIB
CLAVICEPS PURPUREA SCLEROTIUM01G9XEA93NACTIB
BARIUM CARBONATE6P669D8HQ8ACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
GELSEMIUM SEMPERVIRENS ROOT639KR60Q1QACTIB
POTASSIUM PHOSPHATE, DIBASICCI71S98N1ZACTIB
LYCOPODIUM CLAVATUM SPOREC88X29Y479ACTIB
DELPHINIUM STAPHISAGRIA SEED00543AP1JVACTIB
WATER059QF0KO0RIACT
ALCOHOL3K9958V90MIACT

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
CerebraparBAPTISIA TINCTORIA, CEREBRUM SUIS, SECALE CORNUTUM, BARYTA CARBONICA, CALCAREA CARBONICA, GELSEMIUM SEMPERVIRENS, KALI PHOSPHORICUM, LYCOPODIUM CLAVATUM, STAPHYSAGRIAEnergique, Inc.cf6b59ee-64dc-4126-ade9-a92b4c7a3af92024-10-24WarningsExact identifier
ndc (package): 44911-0317-1
ndc (product): 44911-0317
ndc11 (package): 44911031701
spl id: c63dccf3-5bbf-4a26-885f-f9c3de29cf4c
spl set id: cf6b59ee-64dc-4126-ade9-a92b4c7a3af9

Reported adverse events (FAERS/openFDA)#

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