Dosage and administration
Adults and children over 12: Spray twice under the tongue 3 times per day. Children 12 and under: Consult a doctor prior to use.
Hemorrhoid Relief
- Manufacturer
- Liddell Laboratories, Inc. | Apotheca Company
- Effective date
- 2022-04-20
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 3
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 22:02:48
Label at a glance#
ProductHemorrhoid Relief
Active ingredientAESCULUS HIPPOCASTANUM FLOWER, ARNICA MONTANA, CALCIUM FLUORIDE, MILK THISTLE, COLLINSONIA CANADENSIS ROOT, HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK, HYDROCHLORIC ACID, KRAMERIA LAPPACEA ROOT
Label structure9 sections
Contacts and useful links#
Websitewww.liddell.net
WWW.LIDDELL.NET
WWW.LIDDELL.NETLabel contents#
Full prescribing information#
ACTIVE INGREDIENTS:
(in each spray) 12.50 % of Aesculus Hippocastanum 1X, Arnica Montana 3X, Calcarea Fluorica 9X, Carduus Marianus 1X, Collinsonia Canadensis 3X, Hamamelis Virginiana 3X, Muriaticum Acidum 6X, Ratanhia 3X.
INDICATIONS:
May temporarily relieve symptoms associated with hemorrhoids.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
WARNINGS:
If symptoms persist for more than 7 days, 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.
KEEP OUT OF REACH OF CHILDREN:
Keep out of reach of children. In case of overdose, get medical help or call a Poison Control Center right away.
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.
INDICATIONS:
May temporarily relieve symptoms associated with hemorrhoids.**
**Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.
INACTIVE INGREDIENTS:
Organic alcohol 23% v/v, Purified water.
QUESTIONS:
DIST. BY LIDDELL LABORATORIES
WOODBINE, IA 51579WWW.LIDDELL.NET 1-800-460-7733
PACKAGE LABEL DISPLAY:
ORAL SPRAYS
LIDDELL
LABORATORIES
EST. 1994
27Hem
Hemorrhoid
Relief
HOMEOPATHIC
1.0 FL. OZ. (30 ml)
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 50845-0226-1 | 2022-04-20 | C162847 | 48780-1 | ba0f9c33-1fca-a910-e053-dadaa90a0b85 | DRUG FACTS: |
| 50845-0226-1 | 2021-01-29 | C162847 | 48780-1 | ba0f9c33-1fca-a910-e053-dadaa90a0b85 | DRUG FACTS: |
Products#
Every source-derived product name is available through these pages.
- Hemorrhoid Relief
- Aesculus Hippocastanum, Arnica Montana, Calcarea Fluorica, Carduus Marianus, Collinsonia Canadensis, Hamamelis Virginiana, Muriaticum Acidum, Ratanhia
- AESCULUS HIPPOCASTANUM FLOWER
- ARNICA MONTANA
- CALCIUM FLUORIDE
- FLUORIDE ION
- MILK THISTLE
- COLLINSONIA CANADENSIS ROOT
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK
- HYDROCHLORIC ACID
- KRAMERIA LAPPACEA ROOT
- WATER
- ALCOHOL
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 50845-0226 | 50845-0226-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| AESCULUS HIPPOCASTANUM FLOWER | KK0Z92II8M | ACTIB |
| ARNICA MONTANA | O80TY208ZW | ACTIB |
| CALCIUM FLUORIDE | O3B55K4YKI | ACTIB |
| MILK THISTLE | U946SH95EE | ACTIB |
| COLLINSONIA CANADENSIS ROOT | O2630F3XDR | ACTIB |
| HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK | T7S323PKJS | ACTIB |
| HYDROCHLORIC ACID | QTT17582CB | ACTIB |
| KRAMERIA LAPPACEA ROOT | P29ZH1A35Z | ACTIB |
| WATER | 059QF0KO0R | IACT |
| ALCOHOL | 3K9958V90M | IACT |
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 |
|---|---|---|---|---|---|---|
| 6b79b1e9-13b6-4748-a4fc-70b1755ded84 | 045d0007-d774-4b07-851b-598e20a7e0d4 | 2022-04-20 | Warnings | 6b79b1e9-13b6-4748-a4fc-70b1755ded84 045d0007-d774-4b07-851b-598e20a7e0d4 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.