Rectum 6X
- Manufacturer
- Uriel Pharmacy, Inc.
- Effective date
- 2021-10-26
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:15:08
Label at a glance#
ProductRectum 6X
Active ingredientSUS SCROFA RECTUM
Label structure9 sections
Contacts and useful links#
Websitewww.urielpharmacy.com
www.urielpharmacy.com
www.urielpharmacy.comLabel contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE.
DOSAGE & ADMINISTRATION SECTION
Take the contents of one ampule under the tongue and hold for 30 seconds, then swallow.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: Rectum (Bovine rectum) 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt
OTC - PURPOSE SECTION
Use: Promotes healthy balance of homologous organs.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
KEEP OUT OF REACH OF CHILDREN.
WARNINGS SECTION
Warnings: Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. Do not use if allergic to any ingredient. Consult a doctor before use for serious conditions or if conditions worsen or persist. If pregnant or nursing, consult a doctor before use.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Uriel, East Troy, WI 53120
www.urielpharmacy.com Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-8384-1 | Rectum 6X | 10 in 1 BOX | LIQUID | 10 | 1 | |
| 48951-8384-1 | Rectum 6X | 1 mL in 1 AMPULE | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-8384 | RECTUM 6X LIQUID [URIEL PHARMACY, INC.] | 1 | Legacy NDC, 2 package rows | 20211028_cf447223-1551-59cc-e053-2a95a90adb2f.zip |
Products#
Every source-derived product name is available through these pages.
- Rectum 6X
- WATER
- SODIUM CHLORIDE
- SUS SCROFA RECTUM
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-8384 | 48951-8384-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| SUS SCROFA RECTUM | QV1358E70N | ACTIB |
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 |
|---|---|---|---|---|---|---|
| cf447223-1552-59cc-e053-2a95a90adb2f | cf447223-1551-59cc-e053-2a95a90adb2f | 2021-10-26 | Warnings | cf447223-1552-59cc-e053-2a95a90adb2f cf447223-1551-59cc-e053-2a95a90adb2f |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.