Anal Gland
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2011-08-01
- Label type
- OTC ANIMAL DRUG LABEL
- Version
- 2
- 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
Anal Gland: Formulated for symptoms associated with anal gland impaction or infection such as anal itching, inflammation, scratching, gnawing and scooting.
DOSAGE & ADMINISTRATION SECTION
Directions: ORAL USE ONLY - SHAKE WELL. 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
Aesculus hipp. 15x, Aloe 15x, Antimon. crud. 15x, Arsenicum alb. 15x, Capsicum 15x, Carbo veg. 15x, Collinsonia 15x, Granatum 15x, Graphites 15x, Lachesis 15x, Mercurius cyanatus 15x, Nat. mur. 15x, Nux vom. 15x, Ratanhia 15x, Rhus toxicodendron 15x, Sanicula 15x, Silicea 15x, Spigelia anth. 15x, Sulphur 15x, Thuja occ. 15x, Echinacea 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 |
|---|---|---|---|---|
| Activated Charcoal | ACTIVE INGREDIENT | 2P3VWU3H10 | 2 | |
| Aloe | ACTIVE INGREDIENT | V5VD430YW9 | 2 | |
| Antimony Trisulfide | ACTIVE INGREDIENT | F79059A38U | 2 | |
| Arsenic Trioxide | ACTIVE INGREDIENT | S7V92P67HO | 2 | |
| Capsicum | ACTIVE INGREDIENT | 00UK7646FG | 2 | |
| Collinsonia Canadensis Root | ACTIVE INGREDIENT | O2630F3XDR | 2 | |
| Echinacea, Unspecified | ACTIVE INGREDIENT | 4N9P6CC1DX | 2 | |
| Graphite | ACTIVE INGREDIENT | 4QQN74LH4O | 2 | |
| Horse Chestnut | ACTIVE INGREDIENT | 3C18L6RJAZ | 2 | |
| Krameria Lappacea Root | ACTIVE INGREDIENT | P29ZH1A35Z | 2 | |
| Lachesis Muta Venom | ACTIVE INGREDIENT | VSW71SS07I | 2 | |
| Mercuric Cyanide | ACTIVE INGREDIENT | RWG7BD1032 | 2 | |
| Punica Granatum Root Bark | ACTIVE INGREDIENT | CLV24I3T1D | 2 | |
| Sanicula Europaea Leaf | ACTIVE INGREDIENT | JYZ6110L9I | 2 | |
| Silicon Dioxide | ACTIVE INGREDIENT | ETJ7Z6XBU4 | 2 | |
| Sodium Chloride | ACTIVE INGREDIENT | 451W47IQ8X | 2 | |
| Spigelia Anthelmia | ACTIVE INGREDIENT | WYT05213GE | 2 | |
| Strychnos Nux-vomica Seed | ACTIVE INGREDIENT | 269XH13919 | 2 | |
| Sulfur | ACTIVE INGREDIENT | 70FD1KFU70 | 2 | |
| Thuja Occidentalis Leafy Twig | ACTIVE INGREDIENT | 1NT28V9397 | 2 | |
| Toxicodendron Pubescens Leaf | ACTIVE INGREDIENT | 6IO182RP7A | 2 | |
| Activated Charcoal | ACTIVE MOIETY | 2P3VWU3H10 | 2 | |
| Aloe | ACTIVE MOIETY | V5VD430YW9 | 2 | |
| Antimony Trisulfide | ACTIVE MOIETY | F79059A38U | 2 | |
| Arsenic Cation (3+) | ACTIVE MOIETY | C96613F5AV | 2 | |
| Capsicum | ACTIVE MOIETY | 00UK7646FG | 2 | |
| Chloride Ion | ACTIVE MOIETY | Q32ZN48698 | 2 | |
| Collinsonia Canadensis Root | ACTIVE MOIETY | O2630F3XDR | 2 | |
| Echinacea, Unspecified | ACTIVE MOIETY | 4N9P6CC1DX | 2 | |
| Graphite | ACTIVE MOIETY | 4QQN74LH4O | 2 | |
| Horse Chestnut | ACTIVE MOIETY | 3C18L6RJAZ | 2 | |
| Krameria Lappacea Root | ACTIVE MOIETY | P29ZH1A35Z | 2 | |
| Lachesis Muta Venom | ACTIVE MOIETY | VSW71SS07I | 2 | |
| Mercuric Cyanide | ACTIVE MOIETY | RWG7BD1032 | 2 | |
| Punica Granatum Root Bark | ACTIVE MOIETY | CLV24I3T1D | 2 | |
| Sanicula Europaea Leaf | ACTIVE MOIETY | JYZ6110L9I | 2 | |
| Silicon Dioxide | ACTIVE MOIETY | ETJ7Z6XBU4 | 2 | |
| Spigelia Anthelmia | ACTIVE MOIETY | WYT05213GE | 2 | |
| Strychnos Nux-vomica Seed | ACTIVE MOIETY | 269XH13919 | 2 | |
| Sulfur | ACTIVE MOIETY | 70FD1KFU70 | 2 | |
| Thuja Occidentalis Leafy Twig | ACTIVE MOIETY | 1NT28V9397 | 2 | |
| Toxicodendron Pubescens Leaf | ACTIVE MOIETY | 6IO182RP7A | 2 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | 2 |
Products#
Every source-derived product name is available through these pages.
- Anal Gland
- Aesculus hipp., Aloe, Antimon. crud., Arsenicum alb., Capsicum, Carbo veg., Collinsonia, Granatum, Graphites, Lachesis, Mercurius cyanatus, Nat. mur., Nux vom., Ratanhia, Rhus toxicodendron, Sanicula, Silicea, Spigelia anth., Sulphur, Thuja occ., Echinacea
- Horse Chestnut
- Aloe
- Antimony Trisulfide
- Arsenic Trioxide
- Arsenic Cation (3+)
- Capsicum
- Activated Charcoal
- Collinsonia Canadensis Root
- Punica Granatum Root Bark
- Graphite
- Lachesis Muta Venom
- Mercuric Cyanide
- Sodium Chloride
- Chloride Ion
- Strychnos Nux-vomica Seed
- Krameria Lappacea Root
- Toxicodendron Pubescens Leaf
- Sanicula Europaea Leaf
- Silicon Dioxide
- Spigelia Anthelmia
- Sulfur
- Thuja Occidentalis Leafy Twig
- Echinacea, Unspecified
- Alcohol
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-5036 | 55714-5036-1, 55714-5036-3 |
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 | AEROSOL, SPRAY / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TOPICAL | 3633 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / SUBCUTANEOUS | 6.1 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAVENOUS | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CONCENTRATE / BUCCAL | 679 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / RESPIRATORY (INHALATION) | 26664 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / NASAL | 10 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE / ORAL | 882 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAVENOUS | 6405 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVENOUS | 99 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / ORAL | 681 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / SUBCUTANEOUS | 149 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / OPHTHALMIC | 0.5 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / TOPICAL | 561 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SWAB / TOPICAL | 2250 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / TRANSDERMAL | 90 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | POWDER, FOR SOLUTION / TOPICAL | 40 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY, METERED / SUBLINGUAL | 29 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SYRUP / ORAL | 21000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | CAPSULE, EXTENDED RELEASE / ORAL | 8 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / DENTAL | 12.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | JELLY / VAGINAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / ORAL | 6624 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, SPRAY / RESPIRATORY (INHALATION) | 35.75 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TOPICAL | 541 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAMUSCULAR | 1491 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TRANSDERMAL | 49.37 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / ORAL | 3563 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SHAMPOO / TOPICAL | 714 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, EMULSION / INTRAVENOUS | 520 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | DROPS / ORAL | 210 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, FOAM / TOPICAL | 4504 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / RESPIRATORY (INHALATION) | 5 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | TABLET, DELAYED RELEASE / ORAL | NA | ||
| Alcohol | ALCOHOL | 3K9958V90M | SUSPENSION / RECTAL | 0.35 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | LOTION / TOPICAL | 25 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / INTRAVESICAL | 7892 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / TOPICAL | 2445 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | PASTE / DENTAL | 1.8 %w/w | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION / RESPIRATORY (INHALATION) | 0.08 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / INTRAVENOUS | 4000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TRANSDERMAL | 7360 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | MOUTHWASH / BUCCAL | 200 mg/1ml | ||
| Alcohol | ALCOHOL | 3K9958V90M | LIQUID / INTRAMUSCULAR | 400 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION, SOLUTION / INTRAMUSCULAR | 1000 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL, METERED / NASAL | 70 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVENOUS | 92 %w/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL, METERED / TRANSDERMAL | 3675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / TOPICAL | 9971 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | AEROSOL / NASAL | 20 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | GEL / RECTAL | 898 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SPRAY / SUBLINGUAL | 397 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | INJECTION / INTRAVASCULAR | 100 %v/v | ||
| Alcohol | ALCOHOL | 3K9958V90M | ELIXIR / ORAL | 13675 mg | ||
| Alcohol | ALCOHOL | 3K9958V90M | SOLUTION, CONCENTRATE / ORAL | 150.68 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 |
|---|---|---|---|---|---|---|
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | c0f17810-794a-11e6-86a9-424c58303031 | 2026-02-02 | HORSE CHESTNUT | |
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | 84b2f5b1-ce8a-b2a1-e053-2991aa0ac22b | 2025-08-18 | HORSE CHESTNUT | |
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | 84b31246-1ec3-7ef7-e053-2a91aa0a6bfb | 2025-08-18 | HORSE CHESTNUT | |
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | 84111af2-4e09-72cc-e053-2a91aa0ad47a | 2025-07-01 | HORSE CHESTNUT | |
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | 841163a1-d85a-f69d-e053-2991aa0a7e2a | 2025-07-01 | HORSE CHESTNUT | |
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | 8410dc8b-382c-8f38-e053-2a91aa0a850d | 2025-07-01 | HORSE CHESTNUT | |
| Aesculus hippocastanum | HORSE CHESTNUT | Boiron | 84110a8e-83ed-21f4-e053-2991aa0aa128 | 2025-07-01 | HORSE CHESTNUT | |
| Aesculus Hipp Kit Refill | HORSE CHESTNUT | Washington Homeopathic Products | de49ce14-eb8f-4c00-e053-2995a90a2f9f | 2025-01-28 | Warnings | HORSE CHESTNUT |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
