Cedar X Formula

Manufacturer: Integrative Healing Institute, LLC
Effective date: 2025-10-17
Label type: HUMAN OTC DRUG LABEL
Version: 6
Source: full-release
Hydrated at: 2026-06-01 02:37:08

Label at a glance#

ProductCedar X Formula

Active ingredientFRANKINCENSE, THUJA OCCIDENTALIS LEAFY TWIG, GELSEMIUM SEMPERVIRENS ROOT, ONION, ANTIMONY POTASSIUM TARTRATE, CALCIUM SULFIDE, JUNIPER BERRY

Label structure10 sections

Contacts and useful links#

PhoneLabel contact1.888.841.4034

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Active ingredients:Olibanum 3X, Thuja Occidentalis 3X, Gelsemium Sempervirens 4X, Allium Cepa 6C, Antimonium Tartaricum 6C, Hepar Sulphuris Calcareum 6C, Juniperus Communis 30C.

OTC - PURPOSE SECTION

Purpose:Relief from sinus congestion, sneezing, runny nose, red itchy eyes, fatigue, wheezing and coughing.

INDICATIONS & USAGE SECTION

Use:This product is a Homeopathic Dilution, formulated to support the body's immunity for the temporary relief of cedar allergies.

WARNINGS SECTION

Warnings:

Use only as directed.
Stop use and consult a doctor ifsymptoms worsen or do not improve after 5 days.
If pregnant or breast-feeding,ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children.

DOSAGE & ADMINISTRATION SECTION

Directions:Shake bottle well before use.

Adults (12 and Older)Take 10 drops orally 1-3 times a day as needed.
Children (11 and Younger)Take 6 drops orally 1-3 times a day as needed or as directed by your health care provider.
Consult a Physicianfor use in children under 12 years of age.

OTHER SAFETY INFORMATION

Other information:

Do not use if TAMPER EVIDENT seal around neck is broken or missing.
Store at room temperature.

INACTIVE INGREDIENT SECTION

Inactive ingredients:Citric Acid, Potassium Sorbate, Purified Water.

OTHER SAFETY INFORMATION

Mfg. by:OHM Pharma, Inc., Mineral Wells, TX 76067

Made in USA

OTC - QUESTIONS SECTION

INTEGRATIVE HEALING INSTITUTE

San Antonio, TX 78216

integrativehealingsa.com

1.888.841.4034

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

INTEGRATIVE HEALING INSTITUTE

HOMEOPATHIC MEDICINE

NDC: 59623-006-01

NDC: 59623-006-02

CEDAR X FORMULA

SAFE

NATURAL

EFFECTIVE

ALCOHOL FREE

NET 1 fl oz (30 mL)

NET 2 fl oz (60 mL)

1oz bottle label

2oz bottle label

Product Linked Resources#

Resource, Code type, Value table
Resource	Code type	Value	Equivalent identifiers	Source image
Barcode	EAN-13	0000309508283	GTIN-13: 0000309508283 EAN-13: 0000309508283 GTIN-12: 000309508283 UPC-A: 000309508283 GTIN storage (14 digits): 00000309508283	Cedar X Formula 1oz bottle label.jpg
Barcode	EAN-13	0000309508627	GTIN-13: 0000309508627 EAN-13: 0000309508627 GTIN-12: 000309508627 UPC-A: 000309508627 GTIN storage (14 digits): 00000309508627	Cedar X Formula 2oz bottle label.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
59623-006-01	Cedar X Formula	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		6
59623-006-02	Cedar X Formula	59 mL in 1 BOTTLE, DROPPER	LIQUID	59		6

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ANTIMONY POTASSIUM TARTRATE	ACTIVE INGREDIENT	DL6OZ476V3	2
CALCIUM SULFIDE	ACTIVE INGREDIENT	1MBW07J51Q	2
FRANKINCENSE	ACTIVE INGREDIENT	R9XLF1R1WM	2
GELSEMIUM SEMPERVIRENS ROOT	ACTIVE INGREDIENT	639KR60Q1Q	2
JUNIPER BERRY	ACTIVE INGREDIENT	O84B5194RL	2
ONION	ACTIVE INGREDIENT	492225Q21H	2
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE INGREDIENT	1NT28V9397	2
ANTIMONY CATION (3+)	ACTIVE MOIETY	069647RPT5	2
CALCIUM SULFIDE	ACTIVE MOIETY	1MBW07J51Q	2
FRANKINCENSE	ACTIVE MOIETY	R9XLF1R1WM	2
GELSEMIUM SEMPERVIRENS ROOT	ACTIVE MOIETY	639KR60Q1Q	2
JUNIPER BERRY	ACTIVE MOIETY	O84B5194RL	2
ONION	ACTIVE MOIETY	492225Q21H	2
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE MOIETY	1NT28V9397	2
CITRIC ACID MONOHYDRATE	INACTIVE INGREDIENT	2968PHW8QP	2
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	2
WATER	INACTIVE INGREDIENT	059QF0KO0R	2

Products#

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

DailyMed product names page 1 of 1 · 13 matching rows.

Cedar X Formula
Olibanum, Thuja Occidentalis, Gelsemium Sempervirens, Allium Cepa, Antimonium Tartaricum, Hepar Sulphuris Calcareum, Juniperus Communis.
WATER
CITRIC ACID MONOHYDRATE
POTASSIUM SORBATE
FRANKINCENSE
THUJA OCCIDENTALIS LEAFY TWIG
GELSEMIUM SEMPERVIRENS ROOT
ONION
ANTIMONY POTASSIUM TARTRATE
ANTIMONY CATION (3+)
CALCIUM SULFIDE
JUNIPER BERRY

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
59623-006	59623-006-01, 59623-006-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
WATER	059QF0KO0R	IACT
CITRIC ACID MONOHYDRATE	2968PHW8QP	IACT
POTASSIUM SORBATE	1VPU26JZZ4	IACT
FRANKINCENSE	R9XLF1R1WM	ACTIB
THUJA OCCIDENTALIS LEAFY TWIG	1NT28V9397	ACTIB
GELSEMIUM SEMPERVIRENS ROOT	639KR60Q1Q	ACTIB
ONION	492225Q21H	ACTIB
ANTIMONY POTASSIUM TARTRATE	DL6OZ476V3	ACTIB
CALCIUM SULFIDE	1MBW07J51Q	ACTIB
JUNIPER BERRY	O84B5194RL	ACTIB

Source Document#

Source XML

Older Hydrated Versions#

Version, Effective date, Source table
Version	Effective date	Source	Hydrated
5	2021-12-29	full-release	2026-06-01 02:15:24

Inactive ingredient matches#

Inactive Ingredient Database values describe FDA-listed use contexts. The match method and ambiguity count are shown because ingredient names, routes, and dosage forms are not always unique. Browse recovered IID releases and source provenance.

Inactive ingredient links page 1 of 1 · 39 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / ORAL	1000 mg/15ml		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / ORAL	1000 mg/15ml		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	PASTE / ORAL		48 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION / ORAL	1000 mg/15ml		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CAPSULE / ORAL	NA		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	PASTE / ORAL		48 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii+route 36 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	LIQUID / ORAL		114 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CONCENTRATE / ORAL		1 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	GRANULE, FOR SUSPENSION / ORAL		80 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CAPSULE / ORAL	NA		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	GRANULE, FOR SUSPENSION / ORAL		80 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	GRANULE, FOR SUSPENSION / ORAL		80 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CONCENTRATE / ORAL		1 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CONCENTRATE / ORAL		1 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CAPSULE / ORAL	NA		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	PASTE / ORAL		48 mg	Exact identifier — unii+route 36 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	LIQUID / ORAL		114 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii+route 36 equally ranked IID candidates
CITRIC ACID MONOHYDRATE	CITRIC ACID MONOHYDRATE	2968PHW8QP	LIQUID / ORAL		114 mg	Exact identifier — unii+route+dosage form 3 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, FILM COATED, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii+route 36 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii+route 36 equally ranked IID candidates

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
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Cedar X Formula	OLIBANUM, THUJA OCCIDENTALIS, GELSEMIUM SEMPERVIRENS, ALLIUM CEPA, ANTIMONIUM TARTARICUM, HEPAR SULPHURIS CALCAREUM, JUNIPERUS COMMUNIS.	Integrative Healing Institute, LLC	8ab87e13-99ad-4b25-a0c3-e46a868cc684	2025-10-17	Warnings	Exact identifier ndc (package): 59623-006-01 ndc (package): 59623-006-02 ndc (product): 59623-006 ndc11 (package): 59623000601 ndc11 (package): 59623000602 spl id: 4161c4fe-abe4-30ef-e063-6294a90aa911 spl set id: 8ab87e13-99ad-4b25-a0c3-e46a868cc684

Reported adverse events (FAERS/openFDA)#

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