Obsidian by Professional Complementary Health Formulas / Natural Pharmaceutical Manufacturing LLC UOB

Obsidian by

Drug Labeling and Warnings

Obsidian 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]

OBSIDIAN 8135- obsidian 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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UOB

ACTIVE INGREDIENTS

Obsidian 6X, 8X, 12X, 30X

QUESTIONS

Professional Formulas

PO Box 2034 Lake Oswego, OR 97035

INDICATIONS

Temporarily relieves stubbornness, intolerance, feeling ungrounded or detached, anger, being overly critical or judgmental, or fear.*

*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

Obsidian

Homeopathic Remedy

2 FL. OZ. (59 mL)

OBSIDIAN  8135
obsidian liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 63083-8135
Route of Administration	ORAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ)	PROPRANOLOL HYDROCHLORIDE	6 [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: 63083-8135-2	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(63083-8135)

Revised: 1/2026

Document Id: 8ce37fd5-3005-411f-8856-826308f3f738

34390-5

Set id: 684ce0de-33c3-4f84-8cfc-42a7f49137e5

Version: 2

Effective Time: 20260108

 

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