Gulf Detox

Manufacturer
Professional Complementary Health Formulas | Natural Pharmaceutical Manufacturing LLC
Effective date
2019-08-15
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 02:17:17

Label at a glance#

ProductGulf Detox 6038
Active ingredientARCTIUM LAPPA ROOT OIL, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE FLOWER, CHLOROPHYLL, ANTHRACENE, BENZENE, XYLENE (MIXED ISOMERS), PROPYLENE GLYCOL, LIQUID PETROLEUM, POLYCYCLIC AROMATIC HYDROCARBONS
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

Arctium lappa 3X
Taraxacum officinale 3X
Trifolium pratense 3X
Chlorophyllum 6X
Anthracene 30X
Benzene 30X
Xylene 30X
Dispersant isode combination 12X, 30X, 60X, 100X
Gulf water 12X, 30X, 60X, 100X
Petroleum 12X, 30X, 60X, 100X
Hydrocarbons (various) 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, wheezing, eye, nose, or throat irritation, watery or itchy eyes, occasional headache, nausea, sore throat, fatigue, or tiredness due to sensitivity to or exposure to contaminants found in oil spills.*

OTC - PURPOSE SECTION

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

WARNINGS

WARNINGS SECTION

Consult a doctor if condition worsens or symptoms persist. 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

Gulf Detox

Homeopathic Remedy

2 FL. OZ. (59 mL)

Label imageLabel image

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63083-6038-22026-01-08C16284748780-11030e365-1600-111a-e063-dadaa90a10e2X38
63083-6038-22024-01-30C16284748780-11030e365-1600-111a-e063-dadaa90a10e2X38

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63083-6038GULF DETOX 6038 (GULF DETOX) LIQUID [PROFESSIONAL COMPLEMENTARY HEALTH FORMULAS]1Legacy NDC20220406_b308ca7b-0932-49e2-bdfe-e26ab0bdb2c2.zip

Products#

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

DailyMed product names page 1 of 1 · 14 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
63083-603863083-6038-2

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

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
2dd4af75-02cf-4beb-87e4-0bbc83a561f4b308ca7b-0932-49e2-bdfe-e26ab0bdb2c22026-01-08WarningsExact identifier
spl set id: b308ca7b-0932-49e2-bdfe-e26ab0bdb2c2

Reported adverse events (FAERS/openFDA)#

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