FDA.reportPublic FDA data

Industriox

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 17:50:34

Label at a glance#

ProductIndustriox 6011
Active ingredientBERBERIS VULGARIS ROOT BARK, TARAXACUM OFFICINALE, AMMONIUM CATION, CAMPHOR (NATURAL), STRYCHNOS NUX-VOMICA SEED, SULFURIC ACID, OYSTER SHELL CALCIUM CARBONATE, CRUDE, LACHESIS MUTA VENOM, LEAD, ACETONE, ACRYLIC ACID, BENZENE, CARBON TETRACHLORIDE, CHLOROFORM, METHYL ETHYL KETONE, FORMALDEHYDE SOLUTION, TERT-BUTYL METHYL ETHER, NAPHTHALENE, LIQUID PETROLEUM, TRICHLOROETHYLENE
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

Berberis vulgaris 3X
Taraxacum officinale 3X
Ammonium carbonicum 6X
Camphora 6X
Nux vomica 6X
Sulphuricum acidum 6X, 12X
Calcarea carbonica 12X
Lachesis mutus 12X
Plumbum metallicum 12X
Acetonum 30X, 60X
Acrylic resins 30X, 60X
Benzinum 30X, 60X
Carboneum chloratum 30X, 60X
Chloroformum 30X, 60X
Ethylmethyl ketone 30X, 60X
Formalinum 30X, 60X
Gasoline (MTBE) 30X, 60X
Naphthalinum 30X, 60X
Petroleum 30X, 60X
Trichloroethylene 30X, 60X

QUESTIONS

OTC - QUESTIONS SECTION

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

INDICATIONS & USAGE SECTION

For the temporary relief of fatigue, lethargy, headaches, muscle or joint pain, mild bloating or gas, disturbed sleep, or lack of concentration due to sensitivity to or exposure to industrial chemicals, paint, petroleum, steel, and plastics.*

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

Industriox

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-6011-22026-01-09C16284748780-11030e365-58d4-111a-e063-dadaa90a10e2X11
63083-6011-22026-01-09C16284748780-11030e365-58d4-111a-e063-dadaa90a10e2X11
63083-6011-22024-01-30C16284748780-11030e365-58d4-111a-e063-dadaa90a10e2X11
63083-6011-22024-01-30C16284748780-11030e365-58d4-111a-e063-dadaa90a10e2X11

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
63083-6011-2Industriox601159 mL in 1 BOTTLE, DROPPERLIQUID592

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-601163083-6011-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Name, UNII, Kind table
NameUNIIKind
BERBERIS VULGARIS ROOT BARK1TH8Q20J0UACTIB
TARAXACUM OFFICINALE39981FM375ACTIB
AMMONIUM CATION54S68520I4ACTIB
CAMPHOR (NATURAL)N20HL7Q941ACTIB
STRYCHNOS NUX-VOMICA SEED269XH13919ACTIB
SULFURIC ACIDO40UQP6WCFACTIB
OYSTER SHELL CALCIUM CARBONATE, CRUDE2E32821G6IACTIB
LACHESIS MUTA VENOMVSW71SS07IACTIB
LEAD2P299V784PACTIB
ACETONE1364PS73AFACTIB
ACRYLIC ACIDJ94PBK7X8SACTIB
BENZENEJ64922108FACTIB
CARBON TETRACHLORIDECL2T97X0V0ACTIB
CHLOROFORM7V31YC746XACTIB
METHYL ETHYL KETONE6PT9KLV9IOACTIB
FORMALDEHYDE SOLUTIONT0H3L6C7I5ACTIB
TERT-BUTYL METHYL ETHER29I4YB3S89ACTIB
NAPHTHALENE2166IN72UNACTIB
LIQUID PETROLEUM6ZAE7X688JACTIB
TRICHLOROETHYLENE290YE8AR51ACTIB
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
VersionEffective dateSourceHydrated
12019-08-15full-release2026-06-01 02:17:16

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
Industriox 6011INDUSTRIOXProfessional Complementary Health Formulasff4e04ce-6bff-419b-bb6b-d5e97b9942832026-01-08WarningsExact identifier
ndc (package): 63083-6011-2
ndc (product): 63083-6011
ndc11 (package): 63083601102
spl id: ef910ff0-f6b2-40ce-81d8-230a4c6a795e
spl set id: ff4e04ce-6bff-419b-bb6b-d5e97b994283

Reported adverse events (FAERS/openFDA)#

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