Beautox

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 17:49:35

Label at a glance#

ProductBeautox 6007
Active ingredientECHINACEA ANGUSTIFOLIA WHOLE, BOS TAURUS BRAIN, CAMPHOR (NATURAL), BEEF KIDNEY, BEEF LIVER, BEEF LUNG, BOS TAURUS PITUITARY GLAND, POSTERIOR, NITRIC ACID, PHOSPHORIC ACID, ACETYLDIGITOXIN
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

Echinacea angustifolia 2X
Brain 6X
Camphora 6X
Kidney 6X
Liver 6X
Lung 6X
Hypophysis 12X
Nitricum acidum 12X
Phosphoricum acidum 12X
Cosmetologic toxins 30X, 60X, 100X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of cough, shortness of breath, irritation of the eyes, nose, or throat, itchy, dry, or irritated skin, dizziness, or occasional headache due to sensitivity to or exposure to chemicals used in cosmetology.*

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

20% ethanol, purified water.

LABEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Est 1985

Professional Formulas

Complementary Health

Beautox

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-6007-22026-01-09C16284748780-11030e365-0542-111a-e063-dadaa90a10e2X7
63083-6007-22026-01-09C16284748780-11030e365-0542-111a-e063-dadaa90a10e2X7
63083-6007-22024-01-30C16284748780-11030e365-0542-111a-e063-dadaa90a10e2X7
63083-6007-22024-01-30C16284748780-11030e365-0542-111a-e063-dadaa90a10e2X7

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-6007-2Beautox600759 mL in 1 BOTTLE, DROPPERLIQUID592

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
63083-600763083-6007-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 12 matching rows.

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:17:15

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
Beautox 6007BEAUTOXProfessional Complementary Health Formulasd9d2ebff-402e-4393-b262-380410471f1a2026-01-08WarningsExact identifier
ndc (package): 63083-6007-2
ndc (product): 63083-6007
ndc11 (package): 63083600702
spl id: eba53af1-b165-4563-ab42-71e8acff8a19
spl set id: d9d2ebff-402e-4393-b262-380410471f1a

Reported adverse events (FAERS/openFDA)#

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