Female Fibroids
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2011-06-01
- Label type
- HUMAN PRESCRIPTION DRUG LABEL
- Version
- 2
- Source
- full-release
- Hydrated at
- 2026-06-01 02:04:57
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
FEMALE FIBROIDS Formulated for symptoms associated with non-malignant uterine or ovarian fibroids, ovarian or vaginal cysts and uterine polyps.
DOSAGE & ADMINISTRATION SECTION
Directions: ORAL USE ONLY - SHAKE WELL. Ages 12 and up, take 6 drops orally one to four times daily or as directed by a healthcare professional.
ACTIVE INGREDIENT SECTION
Arsenicum alb. 15x, Calcarea iodata 15x, Carbo animalis 15x, Conium 15x, Graphites 15x, Hydrastis 15x, Iodium 15x, Kreosotum 15x, Lachesis 15x, Phosphorus 15x, Sabina 15x, Secale 15x, Sepia 15x, Silicea 15x, Thlaspi 15x, Thuja occ. 15x, Thyroidinum 15x, Trillium pendulum 15x, Ustilago maidis 15x, Hydrastis 3x, Thuja occ. 3x.
PURPOSE SECTION
Formulated for symptoms associated with non-malignant uterine or ovarian fibroids, ovarian or vaginal cysts and uterine polyps.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane dispensing alcohol 20%.
QUESTIONS? SECTION
www.newtonlabs.net Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012
Questions? 1.800.448.7256
WARNINGS SECTION
Warning: Do not use if tamper - evident seal is broken or missing. Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days. Keep out of reach of children.
PREGNANCY OR BREAST FEEDING SECTION
Consult a licensed healthcare professional if pregnant or nursing or if symptoms worsen or persist for more than a few days.
KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
PACKAGE LABEL
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55714-4592-1 | 2020-01-31 | C162847 | 48780-1 | 9d75b9cf-fffe-f424-e053-dadaa90a57ce | Female Fibroids |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 55714-4592-1 | Female Fibroids | 29.57 mL in 1 BOTTLE, GLASS | LIQUID | 29.57 | 2 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 55714-4592 | FEMALE FIBROIDS (ARSENICUM ALB., CLACAREA IODATA, CARBO ANIMALIS, CONIUM, GRAPHITES, HYDRASTIS, IODIUM, KREOSOTUM, LACHESIS, PHOSPHORUS, SABINA, SECALE, SEPIA, SILICEA, THLASPI, THUJA OCC., THYROIDINUM, TRILLIUM PENDULUM, USTILAGO MAIDIS) LIQUID [NEWTON LABORATORIES, INC.] | 2 | Legacy NDC, 1 package rows | 20130912_3e3a703b-7fe3-7b9e-478e-f18638f65240.zip |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Arsenic Trioxide | ACTIVE INGREDIENT | S7V92P67HO | 2 | |
| Calcium Iodide | ACTIVE INGREDIENT | 8EKI9QEE2H | 2 | |
| Capsella Bursa-pastoris | ACTIVE INGREDIENT | W0X9457M59 | 2 | |
| Carbo Animalis | ACTIVE INGREDIENT | 279O8I0433 | 2 | |
| Claviceps Purpurea Sclerotium | ACTIVE INGREDIENT | 01G9XEA93N | 2 | |
| Conium Maculatum Flowering Top | ACTIVE INGREDIENT | Q28R5GF371 | 2 | |
| Goldenseal | ACTIVE INGREDIENT | ZW3Z11D0JV | 2 | |
| Graphite | ACTIVE INGREDIENT | 4QQN74LH4O | 2 | |
| Iodine | ACTIVE INGREDIENT | 9679TC07X4 | 2 | |
| Juniperus Sabina Leafy Twig | ACTIVE INGREDIENT | Z5BEX9K2G1 | 2 | |
| Lachesis Muta Venom | ACTIVE INGREDIENT | VSW71SS07I | 2 | |
| Phosphorus | ACTIVE INGREDIENT | 27YLU75U4W | 2 | |
| Sepia Officinalis Juice | ACTIVE INGREDIENT | QDL83WN8C2 | 2 | |
| Silicon Dioxide | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 2 | |
| Thuja Occidentalis Leafy Twig | ACTIVE INGREDIENT | 1NT28V9397 | 2 | |
| Thyroid, Unspecified | ACTIVE INGREDIENT | 0B4FDL9I6P | 2 | |
| Trillium Erectum Root | ACTIVE INGREDIENT | AHW6F0T2X0 | 2 | |
| Ustilago Maydis | ACTIVE INGREDIENT | 4K7Z7K7SWG | 2 | |
| Wood Creosote | ACTIVE INGREDIENT | 3JYG22FD73 | 2 | |
| Arsenic Cation (3+) | ACTIVE MOIETY | C96613F5AV | 2 | |
| Calcium Cation | ACTIVE MOIETY | 2M83C4R6ZB | 2 | |
| Capsella Bursa-pastoris | ACTIVE MOIETY | W0X9457M59 | 2 | |
| Carbo Animalis | ACTIVE MOIETY | 279O8I0433 | 2 | |
| Claviceps Purpurea Sclerotium | ACTIVE MOIETY | 01G9XEA93N | 2 | |
| Conium Maculatum Flowering Top | ACTIVE MOIETY | Q28R5GF371 | 2 | |
| Goldenseal | ACTIVE MOIETY | ZW3Z11D0JV | 2 | |
| Graphite | ACTIVE MOIETY | 4QQN74LH4O | 2 | |
| Iodine | ACTIVE MOIETY | 9679TC07X4 | 2 | |
| Juniperus Sabina Leafy Twig | ACTIVE MOIETY | Z5BEX9K2G1 | 2 | |
| Lachesis Muta Venom | ACTIVE MOIETY | VSW71SS07I | 2 | |
| Phosphorus | ACTIVE MOIETY | 27YLU75U4W | 2 | |
| Sepia Officinalis Juice | ACTIVE MOIETY | QDL83WN8C2 | 2 | |
| Silicon Dioxide | ACTIVE MOIETY | ETJ7Z6XBU4 | 2 | |
| Thuja Occidentalis Leafy Twig | ACTIVE MOIETY | 1NT28V9397 | 2 | |
| Thyroid, Unspecified | ACTIVE MOIETY | 0B4FDL9I6P | 2 | |
| Trillium Erectum Root | ACTIVE MOIETY | AHW6F0T2X0 | 2 | |
| Ustilago Maydis | ACTIVE MOIETY | 4K7Z7K7SWG | 2 | |
| Wood Creosote | ACTIVE MOIETY | 3JYG22FD73 | 2 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | 2 |
Products#
Every source-derived product name is available through these pages.
- Female Fibroids
- Arsenicum alb., clacarea iodata, Carbo animalis, Conium, Graphites, Hydrastis, Iodium, Kreosotum, Lachesis, Phosphorus, Sabina, Secale, Sepia, Silicea, Thlaspi, Thuja occ., Thyroidinum, Trillium pendulum, Ustilago maidis
- Arsenic Trioxide
- Arsenic Cation (3+)
- Calcium Iodide
- Calcium Cation
- Carbo Animalis
- Conium Maculatum Flowering Top
- Graphite
- Goldenseal
- Iodine
- Wood Creosote
- Lachesis Muta Venom
- Phosphorus
- Juniperus Sabina Leafy Twig
- Claviceps Purpurea Sclerotium
- Sepia Officinalis Juice
- Silicon Dioxide
- Capsella Bursa-pastoris
- Thuja Occidentalis Leafy Twig
- Thyroid, Unspecified
- Trillium Erectum Root
- Ustilago Maydis
- Alcohol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-4592 | 55714-4592-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
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 | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / ORAL | 198 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg |
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 |
|---|---|---|---|---|---|---|
| 659200cf-e603-f19a-de8e-509929ececee | 3e3a703b-7fe3-7b9e-478e-f18638f65240 | 2011-06-01 | Warnings | 659200cf-e603-f19a-de8e-509929ececee 3e3a703b-7fe3-7b9e-478e-f18638f65240 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
