Calendula Thuja

Manufacturer: Uriel Pharmacy Inc.
Effective date: 2018-08-10
Label type: HUMAN OTC DRUG LABEL
Version: 3
Source: legacy-cache
Hydrated at: 2026-08-02 00:52:52

Label at a glance#

ProductCalendula Thuja

Active ingredientCALENDULA OFFICINALIS FLOWERING TOP, ECHINACEA, UNSPECIFIED, ORIGANUM MAJORANA WHOLE, LILIUM LANCIFOLIUM WHOLE FLOWERING, THUJA OCCIDENTALIS WHOLE, WOOD CREOSOTE, PULSATILLA VULGARIS, SILVER, CANDIDA ALBICANS

Label structure9 sections

Contacts and useful links#

PhoneLabel contact866.642.2858

Websitewww.urielpharmacy.com

www.urielpharmacy.com

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

Under age 2: Consult a doctor.

DOSAGE & ADMINISTRATION SECTION

Directions: Fill the provided applicator with 2 to 3 grams of gel and apply at bedtime for 14 nights.

OTC - ACTIVE INGREDIENT SECTION

Active Ingredients: Calendula 2X, Echinacea (Purple coneflower) 2X, Marjorana (Marjoram) 2X, Lilium tigrinum (Tiger lily) 3X, Thuja (American arborvitae) 3X, Kreosotum (Creosote) 6X, Pulsatilla (Pasqueflower) 6X, Argentum colloidal (Colloidal silver) 7X, Candida albicans (Yeast) 33X

INACTIVE INGREDIENT SECTION

Inactive Ingredients: Distilled water, Glycerin, Sodium alginate, Lactic acid, Eucalyptus oil, Rosemary oil, Sage oil, Thyme oil, Tea tree oil, Grapefruit seed extract

OTC - PURPOSE SECTION

Use: Temporary relief of vaginal itching and irritation.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF REACH OF CHILDREN.

WARNINGS SECTION

Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions, if conditions worsen or persist, or accidental ingestion occurs. If pregnant or nursing consult a doctor before use. Avoid contact with eyes. Do not use if safety seals on box are broken or missing. BEST WHEN USED WITHIN 30 DAYS OF OPENING.

OTC - QUESTIONS SECTION

Questions? Call 866.642.2858 Made with care by Uriel, East Troy, WI 53120 www.urielpharmacy.com

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Calendula Thuja Gel

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
48951-3204-8	2023-09-25	C162847	48780-1	9d75b9d0-ba61-f424-e053-dadaa90a57ce	Calendula Thuja
48951-3204-8	2020-01-31	C162847	48780-1	9d75b9d0-ba61-f424-e053-dadaa90a57ce	Calendula Thuja

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
CALENDULA OFFICINALIS FLOWERING TOP	ACTIVE INGREDIENT	18E7415PXQ	1
CANDIDA ALBICANS	ACTIVE INGREDIENT	4D7G21HDBC	1
ECHINACEA, UNSPECIFIED	ACTIVE INGREDIENT	4N9P6CC1DX	1
LILIUM LANCIFOLIUM WHOLE FLOWERING	ACTIVE INGREDIENT	X67Z2963PI	1
ORIGANUM MAJORANA WHOLE	ACTIVE INGREDIENT	R40XM3HU5X	1
PULSATILLA VULGARIS	ACTIVE INGREDIENT	I76KB35JEV	1
SILVER	ACTIVE INGREDIENT	3M4G523W1G	1
THUJA OCCIDENTALIS WHOLE	ACTIVE INGREDIENT	5HBV6WCE3N	1
WOOD CREOSOTE	ACTIVE INGREDIENT	3JYG22FD73	1
CALENDULA OFFICINALIS FLOWERING TOP	ACTIVE MOIETY	18E7415PXQ	1
CANDIDA ALBICANS	ACTIVE MOIETY	4D7G21HDBC	1
ECHINACEA, UNSPECIFIED	ACTIVE MOIETY	4N9P6CC1DX	1
LILIUM LANCIFOLIUM WHOLE FLOWERING	ACTIVE MOIETY	X67Z2963PI	1
ORIGANUM MAJORANA WHOLE	ACTIVE MOIETY	R40XM3HU5X	1
PULSATILLA VULGARIS	ACTIVE MOIETY	I76KB35JEV	1
SILVER	ACTIVE MOIETY	3M4G523W1G	1
THUJA OCCIDENTALIS WHOLE	ACTIVE MOIETY	5HBV6WCE3N	1
WOOD CREOSOTE	ACTIVE MOIETY	3JYG22FD73	1
CITRUS PARADISI SEED	INACTIVE INGREDIENT	12F08874Y7	1
EUCALYPTUS OIL	INACTIVE INGREDIENT	2R04ONI662	1
GLYCERIN	INACTIVE INGREDIENT	PDC6A3C0OX	1
LACTIC ACID	INACTIVE INGREDIENT	33X04XA5AT	1
POTASSIUM SORBATE	INACTIVE INGREDIENT	1VPU26JZZ4	1
ROSEMARY OIL	INACTIVE INGREDIENT	8LGU7VM393	1
SAGE OIL	INACTIVE INGREDIENT	U27K0H1H2O	1
SODIUM ALGINATE	INACTIVE INGREDIENT	C269C4G2ZQ	1
THYME OIL	INACTIVE INGREDIENT	2UK410MY6B	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 20 matching rows.

Calendula Thuja
CITRUS PARADISI SEED
CALENDULA OFFICINALIS FLOWERING TOP
ECHINACEA, UNSPECIFIED
ORIGANUM MAJORANA WHOLE
LILIUM LANCIFOLIUM WHOLE FLOWERING
THUJA OCCIDENTALIS WHOLE
WOOD CREOSOTE
PULSATILLA VULGARIS
SILVER
CANDIDA ALBICANS
TEA TREE OIL
WATER
GLYCERIN
SODIUM ALGINATE
LACTIC ACID
EUCALYPTUS OIL
ROSEMARY OIL
SAGE OIL
THYME OIL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
48951-3204	48951-3204-8

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 19 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
CITRUS PARADISI SEED	12F08874Y7	IACT
CALENDULA OFFICINALIS FLOWERING TOP	18E7415PXQ	ACTIB
ECHINACEA, UNSPECIFIED	4N9P6CC1DX	ACTIB
ORIGANUM MAJORANA WHOLE	R40XM3HU5X	ACTIB
LILIUM LANCIFOLIUM WHOLE FLOWERING	X67Z2963PI	ACTIB
THUJA OCCIDENTALIS WHOLE	5HBV6WCE3N	ACTIB
WOOD CREOSOTE	3JYG22FD73	ACTIB
PULSATILLA VULGARIS	I76KB35JEV	ACTIB
SILVER	3M4G523W1G	ACTIB
CANDIDA ALBICANS	4D7G21HDBC	ACTIB
TEA TREE OIL	VIF565UC2G	IACT
WATER	059QF0KO0R	IACT
GLYCERIN	PDC6A3C0OX	IACT
SODIUM ALGINATE	C269C4G2ZQ	IACT
LACTIC ACID	33X04XA5AT	IACT
EUCALYPTUS OIL	2R04ONI662	IACT
ROSEMARY OIL	8LGU7VM393	IACT
SAGE OIL	U27K0H1H2O	IACT
THYME OIL	2UK410MY6B	IACT

Source Document#

Source XML

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 3 · 121 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION / INTRAMUSCULAR		450 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	TABLET, FILM COATED / ORAL	1.55 mg		Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	CONCENTRATE / ORAL		1 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CREAM, AUGMENTED / TOPICAL		55 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	GEL / TRANSDERMAL		500 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CAPSULE / ORAL		3487 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	SUPPOSITORY / VAGINAL	NA		Exact identifier — unii candidate 18 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SOLUTION / OPHTHALMIC	6 %w/v		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	EMULSION / INTRAVENOUS	2.2 %w/v		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SUPPOSITORY / VAGINAL	227.9 mg		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SOLUTION / AURICULAR (OTIC)	63.64 %w/v		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	MOUTHWASH / BUCCAL	100 mg/1ml		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SUSPENSION / ORAL		26208 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SOLUTION / RESPIRATORY (INHALATION)	5 %w/w		Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, EXTENDED RELEASE / ORAL	0.2 mg		Exact identifier — unii candidate 19 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CLOTH / TOPICAL	0.05 mg/mg		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION, SOLUTION / SUBCUTANEOUS	15 %w/v		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	OINTMENT / TOPICAL	NA		Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	EMULSION / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	TABLET / ORAL		42 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	GEL / TOPICAL		500 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	PASTE / ORAL		3822 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SOAP / TOPICAL	0.76 %w/w		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SPRAY, METERED / NASAL		13 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TROCHE / ORAL		525 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET, EXTENDED RELEASE / ORAL		627 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	INJECTION / INTRAVENOUS		2232 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	TABLET / ORAL		480 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SYRUP / ORAL	3 mg/1ml		Exact identifier — unii candidate 8 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SUSPENSION / ORAL		400 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	CREAM / VAGINAL	0.81 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SPONGE / TOPICAL	2 %w/w		Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	POWDER, FOR SUSPENSION / ORAL		19 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	SUSPENSION / ORAL		49 mg	Exact identifier — unii candidate 8 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	LOTION / TOPICAL	5.7 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION / INTRAVENOUS		33750 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION / INTRAVENOUS	225 mg		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	GEL / OPHTHALMIC	0.88 %w/w		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CAPSULE, EXTENDED RELEASE / ORAL		265 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	FILM, EXTENDED RELEASE / BUCCAL		34 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	FILM, EXTENDED RELEASE / TRANSDERMAL	306.2 mg		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	JELLY / VAGINAL	NA		Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SYRUP / ORAL	2 mg/1ml		Exact identifier — unii candidate 19 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	INJECTION, SOLUTION / INTRAVENOUS		87 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SOLUTION / ORAL		32400 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
SODIUM ALGINATE	SODIUM ALGINATE	C269C4G2ZQ	LIQUID / TOPICAL	0.25 %w/w		Exact identifier — unii candidate 8 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	GUM, CHEWING / BUCCAL		230 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	INJECTION / SUBCUTANEOUS		450 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	LOTION / TOPICAL		3990 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET / ORAL		6 mg	Exact identifier — unii candidate 19 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	LOTION / TOPICAL	0.2 %w/w		Exact identifier — unii candidate 19 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	SUSPENSION / TOPICAL	0.7 %w/w		Exact identifier — unii candidate 18 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	SOLUTION/ DROPS / OPHTHALMIC	0.47 %w/v		Exact identifier — unii candidate 19 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	GEL / TOPICAL		30 mg	Exact identifier — unii candidate 18 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CAPSULE, LIQUID FILLED / ORAL		185 mg	Exact identifier — unii candidate 75 equally ranked IID candidates
POTASSIUM SORBATE	POTASSIUM SORBATE	1VPU26JZZ4	TABLET, COATED / ORAL	NA		Exact identifier — unii candidate 19 equally ranked IID candidates
LACTIC ACID	LACTIC ACID	33X04XA5AT	TABLET / ORAL	ADJ PH		Exact identifier — unii candidate 18 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	SPRAY / NASAL	22.3 mg/1ml		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	LIQUID / TOPICAL	2.5 %w/w		Exact identifier — unii candidate 75 equally ranked IID candidates
GLYCERIN	GLYCERIN	PDC6A3C0OX	CONCENTRATE / ORAL		1800 mg	Exact identifier — unii candidate 75 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
063154fc-8365-5d47-e063-6294a90ad23f			029d43dd-1c1d-4f81-a3c4-68191aa07728	2023-09-25	Warnings	Exact identifier spl set id: 029d43dd-1c1d-4f81-a3c4-68191aa07728

Reported adverse events (FAERS/openFDA)#

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