Hemorrhoids
- Manufacturer
- Newton Laboratories, Inc.
- Effective date
- 2020-01-13
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 23:46:25
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Formulated for associated symptoms such as difficult elimination, itching, inflammation, burning pain and pressure.
DOSAGE & ADMINISTRATION SECTION
Directions: Ages 12 and up, take 6 drops by mouth (ages 0 to 11, give 3 drops) one to four times daily or as directed by a health professional. Sensitive persons begin with 1 drop and gradually increase to full dose.
OTC - ACTIVE INGREDIENT SECTION
Equal parts of Aesculus hippocastanum 6x, Echinacea 6x, Solidago virgaurea 6x, Urtica urens 6x, Aesculus hippocastanum 15x, Aloe 15x, Arsenicum album 15x, Bryonia 15x, Calcarea fluorica 15x, Capsicum annuum 15x, Collinsonia canadensis 15x, Crotalus horridus 15x, Hamamelis virginiana 15x, Hydrofluoricum acidum 15x, Hypericum perforatum 15x, Lachesis mutus 15x, Lycopodium clavatum 15x, Millefolium 15x, Naja tripudians 15x, Nux vomica 15x, Paeonia officinalis 15x, Plantago major 15x, Quercus glandium spiritus 15x, Ratanhia 15x, Vipera berus 15x, Elaps corallinus 30x.
OTC - PURPOSE SECTION
Formulated for associated symptoms such as difficult elimination, itching, inflammation, burning pain and pressure.
INACTIVE INGREDIENT SECTION
Inactive Ingredients: USP Purified Water; USP Gluten-free, non-GMO, organic cane alcohol 20%.
QUESTIONS SECTION
newtonlabs.net – Questions? 800.448.7256
Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30013
WARNINGS SECTION
WARNINGS: Keep out of reach of children. Do not use if tamper-evident seal is broken or missing. If symptoms worsen or persist for more than a few days, consult a doctor. If pregnant or breast-feeding, ask a doctor before use.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a doctor before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children
PACKAGE LABEL.
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 55714-2457-1 | 2024-02-05 | C162847 | 48780-1 | d6a99b39-ed78-a426-e053-dadaa90af4c2 | Hemorrhoids 2457L |
| 55714-2457-1 | 2022-01-28 | C162847 | 48780-1 | d6a99b39-ed78-a426-e053-dadaa90af4c2 | Hemorrhoids 2457L |
Products#
Every source-derived product name is available through these pages.
- Hemorrhoids
- Elaps corallinus, Aesculus hipp., Aloe, Arsenicum alb., Bryonia, Calc. fluor., Capsicum, Collinsonia, Crotalus horridus, Hamamelis, Hydrofluoricum acidum, Hypericum, Lachesis, Lycopodium, Millefolium, Naja, Nux vom., Paeonia, Plantago, Quercus glandium spiritus, Ratanhia, Vipera berus, Echinacea, Solidago, Urtica ur.
- ALCOHOL
- MICRURUS CORALLINUS VENOM
- HORSE CHESTNUT
- ALOE
- ARSENIC TRIOXIDE
- ARSENIC CATION (3+)
- BRYONIA ALBA ROOT
- CALCIUM FLUORIDE
- FLUORIDE ION
- CAPSICUM
- COLLINSONIA CANADENSIS ROOT
- CROTALUS HORRIDUS HORRIDUS VENOM
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
- HYDROFLUORIC ACID
- HYPERICUM PERFORATUM
- LACHESIS MUTA VENOM
- LYCOPODIUM CLAVATUM SPORE
- ACHILLEA MILLEFOLIUM
- NAJA NAJA VENOM
- STRYCHNOS NUX-VOMICA SEED
- PAEONIA OFFICINALIS ROOT
- PLANTAGO MAJOR
- QUERCUS ROBUR NUT
- KRAMERIA LAPPACEA ROOT
- VIPERA BERUS VENOM
- ECHINACEA, UNSPECIFIED
- SOLIDAGO VIRGAUREA FLOWERING TOP
- URTICA URENS
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 55714-2457 | 55714-2457-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
Source Document#
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 |
|---|---|---|---|---|---|---|
| 10a82643-8e40-8300-e063-6294a90a4af4 | 9c08db2a-a949-5940-e053-2995a90a19b9 | 2024-02-05 | Warnings | 9c08db2a-a949-5940-e053-2995a90a19b9 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
