Anxiety Fear
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2011-08-01
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 01:37:34
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Anxiety Fear: Formulated for associated symptoms such as aggression, hypersensitivity, tremors, nervous habits and loss of appetite.
DOSAGE & ADMINISTRATION SECTION
Directions: Pets, under 50 lbs., give 3 drops orally (50 to 500 lbs. - 6 drops, over 500 lbs. - 1/2 teaspoon) as needed or as directed by a healthcare professional. Place in mouth or purified water.
ACTIVE INGREDIENT SECTION
Arg. nit. 15x, Bryonia 15x, Coffea cruda 15x, Cypripedium 15x, Gelsemium 15x, Hypericum 15x, Ignatia 15x, Iodium 15x, Kali brom. 15x, Mag. phos. 15x, Nat. mur. 15x, Nux vom. 15x, Sambucus nig. 15x, Sepia 15x, Stramonium 15x, Theridion 15x, Zinc. met. 15x, Chamomilla 3x, Passiflora 3x, Valeriana 3x
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 Socrata Ingredients#
| Ingredient | Type | UNII | SPL version | Uploaded |
|---|---|---|---|---|
| Arabica Coffee Bean | ACTIVE INGREDIENT | 3SW678MX72 | 3 | |
| Bryonia Alba Root | ACTIVE INGREDIENT | T7J046YI2B | 3 | |
| Cypripedium Parvifolum Root | ACTIVE INGREDIENT | 21Y9GZ1LZA | 3 | |
| Datura Stramonium | ACTIVE INGREDIENT | G6W4F0V8Z3 | 3 | |
| Gelsemium Sempervirens Root | ACTIVE INGREDIENT | 639KR60Q1Q | 3 | |
| Hypericum Perforatum | ACTIVE INGREDIENT | XK4IUX8MNB | 3 | |
| Iodine | ACTIVE INGREDIENT | 9679TC07X4 | 3 | |
| Magnesium Phosphate, Dibasic Trihydrate | ACTIVE INGREDIENT | HF539G9L3Q | 3 | |
| Matricaria Recutita | ACTIVE INGREDIENT | G0R4UBI2ZZ | 3 | |
| Passiflora Incarnata Flowering Top | ACTIVE INGREDIENT | CLF5YFS11O | 3 | |
| Potassium Bromide | ACTIVE INGREDIENT | OSD78555ZM | 3 | |
| Sambucus Nigra Flowering Top | ACTIVE INGREDIENT | CT03BSA18U | 3 | |
| Sepia Officinalis Juice | ACTIVE INGREDIENT | QDL83WN8C2 | 3 | |
| Silver Nitrate | ACTIVE INGREDIENT | 95IT3W8JZE | 3 | |
| Sodium Chloride | ACTIVE INGREDIENT | 451W47IQ8X | 3 | |
| Strychnos Ignatii Seed | ACTIVE INGREDIENT | 1NM3M2487K | 3 | |
| Strychnos Nux-vomica Seed | ACTIVE INGREDIENT | 269XH13919 | 3 | |
| Theridion Curassavicum | ACTIVE INGREDIENT | 9Z8D3HEM8L | 3 | |
| Valerian | ACTIVE INGREDIENT | JWF5YAW3QW | 3 | |
| Zinc | ACTIVE INGREDIENT | J41CSQ7QDS | 3 | |
| Arabica Coffee Bean | ACTIVE MOIETY | 3SW678MX72 | 3 | |
| Bromide Ion | ACTIVE MOIETY | 952902IX06 | 3 | |
| Bryonia Alba Root | ACTIVE MOIETY | T7J046YI2B | 3 | |
| Chloride Ion | ACTIVE MOIETY | Q32ZN48698 | 3 | |
| Cypripedium Parvifolum Root | ACTIVE MOIETY | 21Y9GZ1LZA | 3 | |
| Datura Stramonium | ACTIVE MOIETY | G6W4F0V8Z3 | 3 | |
| Gelsemium Sempervirens Root | ACTIVE MOIETY | 639KR60Q1Q | 3 | |
| Hypericum Perforatum | ACTIVE MOIETY | XK4IUX8MNB | 3 | |
| Iodine | ACTIVE MOIETY | 9679TC07X4 | 3 | |
| Magnesium Cation | ACTIVE MOIETY | T6V3LHY838 | 3 | |
| Matricaria Recutita | ACTIVE MOIETY | G0R4UBI2ZZ | 3 | |
| Passiflora Incarnata Flowering Top | ACTIVE MOIETY | CLF5YFS11O | 3 | |
| Sambucus Nigra Flowering Top | ACTIVE MOIETY | CT03BSA18U | 3 | |
| Sepia Officinalis Juice | ACTIVE MOIETY | QDL83WN8C2 | 3 | |
| Silver Cation | ACTIVE MOIETY | 57N7B0K90A | 3 | |
| Strychnos Ignatii Seed | ACTIVE MOIETY | 1NM3M2487K | 3 | |
| Strychnos Nux-vomica Seed | ACTIVE MOIETY | 269XH13919 | 3 | |
| Theridion Curassavicum | ACTIVE MOIETY | 9Z8D3HEM8L | 3 | |
| Valerian | ACTIVE MOIETY | JWF5YAW3QW | 3 | |
| Zinc | ACTIVE MOIETY | J41CSQ7QDS | 3 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | 3 |
Products#
Every source-derived product name is available through these pages.
- Anxiety Fear
- Arg. nit., Bryonia, Coffea cruda, Cypripedium, Gelsemium, Hypericum, Ignatia, Iodium, Kali brom., Mag. phos., Nat. mur., Nux vom., Sambucus nig., Sepia, Stramonium, Theridion, Zinc. met., Chamomilla, Passiflora, Valeriana
- Silver Nitrate
- Silver Cation
- Bryonia Alba Root
- Arabica Coffee Bean
- Cypripedium Parvifolum Root
- Gelsemium Sempervirens Root
- Hypericum Perforatum
- Strychnos Ignatii Seed
- Iodine
- Potassium Bromide
- Bromide Ion
- Magnesium Phosphate, Dibasic Trihydrate
- Magnesium Cation
- Sodium Chloride
- Chloride Ion
- Strychnos Nux-vomica Seed
- Sambucus Nigra Flowering Top
- Sepia Officinalis Juice
- Datura Stramonium
- Theridion Curassavicum
- Zinc
- Matricaria Recutita
- Passiflora Incarnata Flowering Top
- Valerian
- Alcohol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-5004 | 55714-5004-1, 55714-5004-3 |
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 | CONCENTRATE / ORAL | 198 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| 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 | SPRAY / SUBLINGUAL | 397 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
