Candida HP

Manufacturer: Natural Creations, Inc. | OHM Pharma, Inc.
Effective date: 2012-10-16
Label type: HUMAN OTC DRUG LABEL
Version: 1
Source: full-release
Hydrated at: 2026-06-01 02:04:04

Label at a glance#

ProductCandida HP

Active ingredientECHINACEA PURPUREA, BAPTISIA TINCTORIA ROOT, GLYCYRRHIZA GLABRA, ASTRAGALUS NUTTALLII LEAF, SODIUM BORATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, WOOD CREOSOTE, LYCOPODIUM CLAVATUM SPORE, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, NITRIC ACID, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, THUJA OCCIDENTALIS LEAFY TWIG, CANDIDA ALBICANS

Label structure11 sections

Contacts and useful links#

PhoneLabel contact712.647.2780

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ACTIVE INGREDIENTS (HPUS*): Echinacea Purpurea MT, Baptisia Tinctoria 3X, Glycyrrhiza Glabra 3X, Astragalus Menziesii 6X, Borax 30C, Calcarea Carbonica 30C, Kreosotum 30C, Lycopodium Clavatum 30C, Natrum Phosphoricum 30C, Nitricum Acidum 30C, Nux Vomica 30C, Phosphoricum Acidum 30C, Pulsatilla 30C, sepia 30C, Thuja Occidentalis 30C, Candida Albicans 10C, 30C, 200C

INDICATIONS & USAGE SECTION

USES: Temporarily relieves headache, diarrhea, constipation, oral thrush, exhaustion, irritability, leucorrhea, itching & redness of female areas, &/or other symptoms related to a candida infection.

WARNINGS SECTION

WARNING:

Consult a physician for use in children under 12 years of age. IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use. KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

OTC - DO NOT USE SECTION

OTHER INFORMATION: Tamper Seal: "Sealed for your protection.

Do not use if seal is broken or missing.

REFERENCES SECTION

*The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENTS: Purified Water, USP Ethanol Alcohol 20%

OTC - QUESTIONS SECTION

QUESTIONS AND COMMENTS?

MFG FOR: Natural Creations / Woodbine, IA / 51579 712.647.2780

LOT:

OTC - PURPOSE SECTION

USES: Temporarily relieves headache, diarrhea, constipation, oral thrush, exhaustion, irritability, leucorrhea, itching & redness of female areas, &/or other symptoms related to a candida infection.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC: 43406-0011-1

CANDIDA HP

Candida Infection

HOMEOPATHIC

1 fl oz (30 mL) / 20% Ethanol (Alcohol)

UPC: 877730000774

Image Of Label

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
efd58dcf-540a-4531-8766-e713129ca6f2	Product name	1	20250307
4b7700e3-6e0e-45e5-9d22-6f754d61386e	Product name	2	20250304
726062af-1135-4707-a1d7-57256991bbf9	Product name	2	20250226
7cda52fc-125f-421c-8fea-bc1974370c49	Product name	2	20180703
0ca1d589-929b-4b33-bc5b-1d84abdafa6a	Product name	1	20150324
fc363c46-397b-4476-ac0f-70e43e8e4592	Product name	1	20150324
19c71a3d-ed9c-166b-a7e5-38c250c35631	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
43406-0011-1	2019-11-27	C162847	48780-1	9855d018-ef48-cd31-e053-dbdaa90ab51a	CANDIDA HP

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
43406-0011-1	Candida HP	30 mL in 1 BOTTLE, DROPPER	LIQUID	30		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
43406-0011	CANDIDA HP (ECHINACEA PURPUREA, BAPTISIA TINCTORIA ROOT, GLYCYRRHIZA GLABRA, ASTRAGALUS NUTTALLII LEAF, SODIUM BORATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, WOOD CREOSOTE, LYCOPODIUM CLAVATUM SPORE, SODIUM PHOSPHATE, DIBASIC HEPTAHYDRATE, NITRIC ACID, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, PULSATILLA VULGARIS, SEPIA OFFICINALIS JUICE, CANDIDA ALBICANS) LIQUID [NATURAL CREATIONS, INC.]	1	Legacy NDC, 1 package rows	20121018_a6951cde-7c8e-4cc6-ae98-c3b6f66b90d1.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	SPL version
ASTRAGALUS NUTTALLII LEAF	ACTIVE INGREDIENT	NC1P15G4KZ	1
BAPTISIA TINCTORIA ROOT	ACTIVE INGREDIENT	5EF0HWI5WU	1
CANDIDA ALBICANS	ACTIVE INGREDIENT	4D7G21HDBC	1
ECHINACEA PURPUREA	ACTIVE INGREDIENT	QI7G114Y98	1
GLYCYRRHIZA GLABRA	ACTIVE INGREDIENT	2788Z9758H	1
LYCOPODIUM CLAVATUM SPORE	ACTIVE INGREDIENT	C88X29Y479	1
NITRIC ACID	ACTIVE INGREDIENT	411VRN1TV4	1
OYSTER SHELL CALCIUM CARBONATE, CRUDE	ACTIVE INGREDIENT	2E32821G6I	1
PHOSPHORIC ACID	ACTIVE INGREDIENT	E4GA8884NN	1
PULSATILLA VULGARIS	ACTIVE INGREDIENT	I76KB35JEV	1
SEPIA OFFICINALIS JUICE	ACTIVE INGREDIENT	QDL83WN8C2	1
SODIUM BORATE	ACTIVE INGREDIENT	91MBZ8H3QO	1
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE	ACTIVE INGREDIENT	70WT22SF4B	1
STRYCHNOS NUX-VOMICA SEED	ACTIVE INGREDIENT	269XH13919	1
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE INGREDIENT	1NT28V9397	1
WOOD CREOSOTE	ACTIVE INGREDIENT	3JYG22FD73	1
ASTRAGALUS NUTTALLII LEAF	ACTIVE MOIETY	NC1P15G4KZ	1
BAPTISIA TINCTORIA ROOT	ACTIVE MOIETY	5EF0HWI5WU	1
BORATE ION	ACTIVE MOIETY	44OAE30D22	1
CANDIDA ALBICANS	ACTIVE MOIETY	4D7G21HDBC	1
ECHINACEA PURPUREA	ACTIVE MOIETY	QI7G114Y98	1
GLYCYRRHIZA GLABRA	ACTIVE MOIETY	2788Z9758H	1
LYCOPODIUM CLAVATUM SPORE	ACTIVE MOIETY	C88X29Y479	1
NITRIC ACID	ACTIVE MOIETY	411VRN1TV4	1
OYSTER SHELL CALCIUM CARBONATE, CRUDE	ACTIVE MOIETY	2E32821G6I	1
PHOSPHATE ION	ACTIVE MOIETY	NK08V8K8HR	1
PHOSPHORIC ACID	ACTIVE MOIETY	E4GA8884NN	1
PULSATILLA VULGARIS	ACTIVE MOIETY	I76KB35JEV	1
SEPIA OFFICINALIS JUICE	ACTIVE MOIETY	QDL83WN8C2	1
STRYCHNOS NUX-VOMICA SEED	ACTIVE MOIETY	269XH13919	1
THUJA OCCIDENTALIS LEAFY TWIG	ACTIVE MOIETY	1NT28V9397	1
WOOD CREOSOTE	ACTIVE MOIETY	3JYG22FD73	1
ALCOHOL	INACTIVE INGREDIENT	3K9958V90M	1
WATER	INACTIVE INGREDIENT	059QF0KO0R	1

Products#

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

DailyMed product names page 1 of 1 · 22 matching rows.

Candida HP
Echinacea Purpurea, Baptisia Tinctoria Root, Glycyrrhiza Glabra, Astragalus Nuttallii Leaf, Sodium Borate, Oyster Shell Calcium Carbonate, Crude, Wood Creosote, Lycopodium Clavatum Spore, Sodium Phosphate, Dibasic Heptahydrate, Nitric Acid, Strychnos Nux-Vomica Seed, Phosphoric Acid, Pulsatilla Vulgaris, Sepia Officinalis Juice, Candida Albicans
ECHINACEA PURPUREA
BAPTISIA TINCTORIA ROOT
GLYCYRRHIZA GLABRA
ASTRAGALUS NUTTALLII LEAF
SODIUM BORATE
BORATE ION
OYSTER SHELL CALCIUM CARBONATE, CRUDE
WOOD CREOSOTE
LYCOPODIUM CLAVATUM SPORE
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE
PHOSPHATE ION
NITRIC ACID
STRYCHNOS NUX-VOMICA SEED
PHOSPHORIC ACID
PULSATILLA VULGARIS
SEPIA OFFICINALIS JUICE
THUJA OCCIDENTALIS LEAFY TWIG
CANDIDA ALBICANS
WATER
ALCOHOL

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
43406-0011	43406-0011-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 20 matching rows.

Name, UNII, Kind table
Name	UNII	Kind
ECHINACEA PURPUREA	QI7G114Y98	ACTIM
BAPTISIA TINCTORIA ROOT	5EF0HWI5WU	ACTIM
GLYCYRRHIZA GLABRA	2788Z9758H	ACTIM
ASTRAGALUS NUTTALLII LEAF	NC1P15G4KZ	ACTIM
SODIUM BORATE	91MBZ8H3QO	ACTIM
OYSTER SHELL CALCIUM CARBONATE, CRUDE	2E32821G6I	ACTIM
WOOD CREOSOTE	3JYG22FD73	ACTIM
LYCOPODIUM CLAVATUM SPORE	C88X29Y479	ACTIM
SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE	70WT22SF4B	ACTIM
NITRIC ACID	411VRN1TV4	ACTIM
STRYCHNOS NUX-VOMICA SEED	269XH13919	ACTIM
PHOSPHORIC ACID	E4GA8884NN	ACTIM
PULSATILLA VULGARIS	I76KB35JEV	ACTIM
SEPIA OFFICINALIS JUICE	QDL83WN8C2	ACTIM
THUJA OCCIDENTALIS LEAFY TWIG	1NT28V9397	ACTIM
CANDIDA ALBICANS	4D7G21HDBC	ACTIM
CANDIDA ALBICANS	4D7G21HDBC	ACTIM
CANDIDA ALBICANS	4D7G21HDBC	ACTIM
WATER	059QF0KO0R	IACT
ALCOHOL	3K9958V90M	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 1 · 59 matching rows.

DailyMed ingredient, IID ingredient, UNII table
DailyMed ingredient	IID ingredient	UNII	Dosage form / route	Potency	Maximum daily exposure	Match
ALCOHOL	ALCOHOL	3K9958V90M	LOTION / TOPICAL	25 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE / ORAL		882 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / RECTAL	0.35 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SHAMPOO / TOPICAL		714 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / ORAL	150.68 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TRANSDERMAL		3675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / NASAL		20 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SYRUP / ORAL		21000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / SUBCUTANEOUS		149 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAMUSCULAR		1000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAVENOUS		400 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / ORAL	210 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVENOUS	92 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TOPICAL		2445 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / TRANSDERMAL	49.37 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / RECTAL		898 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TOPICAL		9971 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TOPICAL		3633 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, FOAM / TOPICAL		4504 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CAPSULE, EXTENDED RELEASE / ORAL		8 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / TRANSDERMAL		7360 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / TOPICAL		561 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	TABLET, DELAYED RELEASE / ORAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	DROPS / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / NASAL	70 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVESICAL		7892 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	MOUTHWASH / BUCCAL	200 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / SUBCUTANEOUS	6.1 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / NASAL	10 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / OPHTHALMIC	0.5 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / ORAL		3563 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL, METERED / TOPICAL		541 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL / NASAL	20 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	ELIXIR / ORAL		13675 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / RESPIRATORY (INHALATION)	0.08 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION, CONCENTRATE / INTRAVENOUS		4000 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / RESPIRATORY (INHALATION)	5 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAVASCULAR	100 %v/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / BUCCAL	679 mg/1ml		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	JELLY / VAGINAL	NA		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SWAB / TOPICAL		2250 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION / INTRAMUSCULAR		1491 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY, METERED / SUBLINGUAL		29 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	PASTE / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	CONCENTRATE / ORAL	198 mg		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, SOLUTION / INTRAVENOUS		6405 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	INJECTION, EMULSION / INTRAVENOUS		520 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	GEL / DENTAL	1.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / DENTAL	12.8 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SUSPENSION / ORAL		681 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, METERED / RESPIRATORY (INHALATION)		26664 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	AEROSOL, SPRAY / RESPIRATORY (INHALATION)	35.75 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / INTRAVENOUS		99 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / TRANSDERMAL	90 %w/v		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	POWDER, FOR SOLUTION / TOPICAL	40 %w/w		Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SOLUTION / ORAL		6624 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	SPRAY / SUBLINGUAL		397 mg	Exact identifier — unii candidate 59 equally ranked IID candidates
ALCOHOL	ALCOHOL	3K9958V90M	LIQUID / INTRAMUSCULAR		400 mg	Exact identifier — unii candidate 59 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
44f82d12-c64b-4df9-889b-dc87f5883baf			a6951cde-7c8e-4cc6-ae98-c3b6f66b90d1	2012-10-16	Warnings	Exact identifier spl id: 44f82d12-c64b-4df9-889b-dc87f5883baf spl set id: a6951cde-7c8e-4cc6-ae98-c3b6f66b90d1

Reported adverse events (FAERS/openFDA)#

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