Delirium Formula

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 17:50:51

Label at a glance#

ProductDelirium Formula 2116
Active ingredientPAPAYA, SCUTELLARIA BAICALENSIS ROOT, DATURA METEL FLOWER, ACONITUM CARMICHAELI LATERAL ROOT, RANUNCULUS BULBOSUS ROOT
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

Mu-Kua 1X
Huang-Chin 2X
Yang-Chin-Hua 3X
Fu-Tzu 4X
Mao-Chua-Tsao 4X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of confusion or disorientation, memory loss, disorganized thinking, or mood swings.*

OTC - PURPOSE SECTION

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

WARNINGS

WARNINGS SECTION

Severe or persistent symptoms may be serious. Consult a doctor promptly. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

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

20% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Delirium Formula

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-2116-22026-01-09C16284748780-11030e365-6aca-111a-e063-dadaa90a10e2C116
63083-2116-22026-01-09C16284748780-11030e365-6aca-111a-e063-dadaa90a10e2C116
63083-2116-22024-01-30C16284748780-11030e365-6aca-111a-e063-dadaa90a10e2C116
63083-2116-22024-01-30C16284748780-11030e365-6aca-111a-e063-dadaa90a10e2C116

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-2116-2Delirium Formula211659 mL in 1 BOTTLE, DROPPERLIQUID592

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
63083-211663083-2116-2

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

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:16:28

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
Delirium Formula 2116DELIRIUM FORMULAProfessional Complementary Health Formulas178a5115-06c1-4048-832d-b0cdde7bf45b2026-01-08WarningsExact identifier
ndc (package): 63083-2116-2
ndc (product): 63083-2116
ndc11 (package): 63083211602
spl id: e725d46c-2516-4ba2-9f0a-e3cf6c0e0dc8
spl set id: 178a5115-06c1-4048-832d-b0cdde7bf45b

Reported adverse events (FAERS/openFDA)#

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