Paraben Isode Detox by Professional Complementary Health Formulas / Natural Pharmaceutical Manufacturing LLC X40

Paraben Isode Detox by

Drug Labeling and Warnings

Paraben Isode Detox by is a Homeopathic medication manufactured, distributed, or labeled by Professional Complementary Health Formulas, Natural Pharmaceutical Manufacturing LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

PARABEN ISODE DETOX 6040- paraben isode detox liquid 
Professional Complementary Health Formulas

Disclaimer: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.

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X40

ACTIVE INGREDIENTS

Butylparaben 12X, 30X, 60X
Ethylparaben 12X, 30X, 60X
Methylparaben 12X, 30X, 60X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

For the temporary relief of dry, itchy, or irritated skin, bloating, mood swings, difficulty sleeping, or foggy thinking due to sensitivity to or exposure to preservatives found in cosmetic and pharmaceutical products.*

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

WARNINGS

In case of overdose, get medical help or contact a poison control center right away.

Keep out of the reach of children.

If pregnant or breastfeeding, ask a healthcare professional before use.

DIRECTIONS

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

Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

INACTIVE INGREDIENTS

20% ethanol, purified water.

LABEL

Est 1985

Professional Formulas

Complementary Health

Paraben Isode Detox

Homeopathic Remedy

2 FL. OZ. (59 mL)

PARABEN ISODE DETOX  6040
paraben isode detox liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-6040
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
BUTYLPARABEN (UNII: 3QPI1U3FV8) (BUTYLPARABEN - UNII:3QPI1U3FV8)	BUTYLPARABEN	12 [hp_X]  in 59 mL
ETHYLPARABEN (UNII: 14255EXE39) (ETHYLPARABEN - UNII:14255EXE39)	ETHYLPARABEN	12 [hp_X]  in 59 mL
METHYLPARABEN (UNII: A2I8C7HI9T) (METHYLPARABEN - UNII:A2I8C7HI9T)	METHYLPARABEN	12 [hp_X]  in 59 mL

Inactive Ingredients
Ingredient Name	Strength
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 63083-6040-2	59 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product	08/15/1985	01/09/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
unapproved homeopathic		08/15/1984	01/09/2026

Labeler - Professional Complementary Health Formulas (167339027)

Registrant - Natural Pharmaceutical Manufacturing LLC (015624923)

Establishment
Name	Address	ID/FEI	Business Operations
Natural Pharmaceutical Manufacturing LLC		015624923	manufacture(63083-6040)

Revised: 1/2026

Document Id: f9c459fd-087d-42ea-bca6-5ef9ef9a5304

34390-5

Set id: 0fe38ce6-80b2-457a-a940-cc265bae109f

Version: 2

Effective Time: 20260108

 

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