Candida Yeast
- Manufacturer
- Liddell Laboratories, Inc.
- Effective date
- 2021-12-21
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:21:51
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
ACTIVE INGREDIENTS: Baptisia tinctoria 3X, Borax 30C, Candida albicans 12X, Candida parapsilosis 12X, Echinacea 3X, Kreosotum 30C, Mercurius cyanatus 30C, Mercurius sulphuratus ruber 30C, Nitricum acidum 30C, Pyrogenium 200C, Sulphuricum acidum 30C, Thuja occidentalis 30C.
OTC - PURPOSE SECTION
INDICATIONS: Relieves symptoms of Candida infections: vaginal discharge, vaginal discomfort, abdominal distention, bloating.
WARNINGS SECTION
WARNINGS: If symptoms persist, consult a doctor.
If pregnant or breast feeding, ask a doctor before use.
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
Do not use if TAMPER EVIDENT seal around neck of bottle is missing or broken.
DOSAGE & ADMINISTRATION SECTION
DIRECTIONS:Adults and children over 12: Spray twice under the tongue 3 times per day. Children 12 and under: Consult a doctor prior to use.
INACTIVE INGREDIENT SECTION
INACTIVE INGREDIENTS: Organic alcohol 20% v/v, Purified water.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.
INDICATIONS & USAGE SECTION
INDICATIONS: Relieves symptoms of Candida infections: vaginal discharge, vaginal discomfort, abdominal distention, bloating.
OTC - QUESTIONS SECTION
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
ORAL SPRAYS
LIDDELL
LABORATORIES
CAN
Candida Yeast
HOMEOPATHIC
1.0 FL. OZ (30 ml)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0101-1 | 2021-12-21 | C162847 | 48780-1 | 9855d018-e285-cd31-e053-dbdaa90ab51a | Drug Facts |
| 50845-0101-1 | 2019-11-27 | C162847 | 48780-1 | 9855d018-e285-cd31-e053-dbdaa90ab51a | Drug Facts |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| BAPTISIA TINCTORIA ROOT | ACTIVE INGREDIENT | 5EF0HWI5WU | 3 | |
| CANDIDA ALBICANS | ACTIVE INGREDIENT | 4D7G21HDBC | 3 | |
| CANDIDA PARAPSILOSIS | ACTIVE INGREDIENT | 0KZ676D44N | 3 | |
| ECHINACEA, UNSPECIFIED | ACTIVE INGREDIENT | 4N9P6CC1DX | 3 | |
| MERCURIC CYANIDE | ACTIVE INGREDIENT | RWG7BD1032 | 3 | |
| MERCURIC SULFIDE | ACTIVE INGREDIENT | ZI0T668SF1 | 3 | |
| NITRIC ACID | ACTIVE INGREDIENT | 411VRN1TV4 | 3 | |
| RANCID BEEF | ACTIVE INGREDIENT | 29SUH5R3HU | 3 | |
| SODIUM BORATE | ACTIVE INGREDIENT | 91MBZ8H3QO | 3 | |
| SULFURIC ACID | ACTIVE INGREDIENT | O40UQP6WCF | 3 | |
| THUJA OCCIDENTALIS LEAFY TWIG | ACTIVE INGREDIENT | 1NT28V9397 | 3 | |
| WOOD CREOSOTE | ACTIVE INGREDIENT | 3JYG22FD73 | 3 | |
| BAPTISIA TINCTORIA ROOT | ACTIVE MOIETY | 5EF0HWI5WU | 3 | |
| BORATE ION | ACTIVE MOIETY | 44OAE30D22 | 3 | |
| CANDIDA ALBICANS | ACTIVE MOIETY | 4D7G21HDBC | 3 | |
| CANDIDA PARAPSILOSIS | ACTIVE MOIETY | 0KZ676D44N | 3 | |
| ECHINACEA, UNSPECIFIED | ACTIVE MOIETY | 4N9P6CC1DX | 3 | |
| MERCURIC CATION | ACTIVE MOIETY | ED30FJ8Y42 | 3 | |
| MERCURIC CYANIDE | ACTIVE MOIETY | RWG7BD1032 | 3 | |
| NITRIC ACID | ACTIVE MOIETY | 411VRN1TV4 | 3 | |
| RANCID BEEF | ACTIVE MOIETY | 29SUH5R3HU | 3 | |
| SULFURIC ACID | ACTIVE MOIETY | O40UQP6WCF | 3 | |
| THUJA OCCIDENTALIS LEAFY TWIG | ACTIVE MOIETY | 1NT28V9397 | 3 | |
| WOOD CREOSOTE | ACTIVE MOIETY | 3JYG22FD73 | 3 | |
| ALCOHOL | INACTIVE INGREDIENT | 3K9958V90M | 3 | |
| WATER | INACTIVE INGREDIENT | 059QF0KO0R | 3 |
Products#
Every source-derived product name is available through these pages.
- Candida Yeast
- Baptisia tinctoria, Borax, Candida albicans, Candida parapsilosis, Echinacea, Kreosotum, Mercurius cyanatus, Mercurius sulphuratus ruber, Nitricum acidum,
- BAPTISIA TINCTORIA ROOT
- SODIUM BORATE
- BORATE ION
- CANDIDA ALBICANS
- CANDIDA PARAPSILOSIS
- ECHINACEA, UNSPECIFIED
- MERCURIC SULFIDE
- MERCURIC CATION
- MERCURIC CYANIDE
- NITRIC ACID
- RANCID BEEF
- SULFURIC ACID
- THUJA OCCIDENTALIS LEAFY TWIG
- WATER
- ALCOHOL
- WOOD CREOSOTE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50845-0101 | 50845-0101-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| BAPTISIA TINCTORIA ROOT | 5EF0HWI5WU | ACTIB |
| SODIUM BORATE | 91MBZ8H3QO | ACTIB |
| CANDIDA ALBICANS | 4D7G21HDBC | ACTIB |
| CANDIDA PARAPSILOSIS | 0KZ676D44N | ACTIB |
| ECHINACEA, UNSPECIFIED | 4N9P6CC1DX | ACTIB |
| MERCURIC SULFIDE | ZI0T668SF1 | ACTIB |
| MERCURIC CYANIDE | RWG7BD1032 | ACTIB |
| NITRIC ACID | 411VRN1TV4 | ACTIB |
| RANCID BEEF | 29SUH5R3HU | ACTIB |
| SULFURIC ACID | O40UQP6WCF | ACTIB |
| THUJA OCCIDENTALIS LEAFY TWIG | 1NT28V9397 | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
| WOOD CREOSOTE | 3JYG22FD73 | ACTIB |
Source Document#
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.
| DailyMed ingredient | IID ingredient | UNII | Dosage form / route | Potency | Maximum daily exposure | Match |
|---|---|---|---|---|---|---|
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| ALCOHOL | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml |
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| 2cfaba34-a038-4cc6-bcdf-3b4d75c8c798 | f8758765-410b-4990-b485-880aa7129026 | 2021-12-21 | Warnings | 2cfaba34-a038-4cc6-bcdf-3b4d75c8c798 f8758765-410b-4990-b485-880aa7129026 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
