Cinis Equiseti 6
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2024-11-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 7
- Source
- full-release
- Hydrated at
- 2026-06-01 02:28:56
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
INDICATIONS & USAGE SECTION
Directions: FOR ORAL USE ONLY.
DOSAGE & ADMINISTRATION SECTION
Take 3-4 times daily. Ages 12 and older: 10 drops. Ages 2-11: 5 drops. Under age 2: Consult a doctor.
OTC - ACTIVE INGREDIENT SECTION
Active Ingredient: Cinis equiseti (Ash of horsetail herb) 6X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Distilled water, 20% Organic cane alcohol, Lactose
Prepared using rhythmical processes.
OTC - PURPOSE SECTION
Use: Temporary relief of headache.
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. Contains traces of lactose. If pregnant or nursing, consult a doctor before use. Do not use if safety seal is broken or missing.
OTC - QUESTIONS SECTION
Questions? Call 866.642.2858
Made with care by Uriel, East Troy, WI 53120
shopuriel.com Lot:
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-3235-3 | Cinis Equiseti 6 | 60 mL in 1 BOTTLE, DROPPER | LIQUID | 60 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-3235 | CINIS EQUISETI 6 LIQUID [URIEL PHARMACY INC.] | 7 | Legacy NDC, 1 package rows | 20241116_b633713a-35fd-11e4-e053-2a95a90a3e1d.zip |
Products#
Every source-derived product name is available through these pages.
- Cinis Equiseti 6
- EQUISETUM ARVENSE TOP
- LACTOSE, UNSPECIFIED FORM
- WATER
- SUCROSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-3235 | 48951-3235-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| EQUISETUM ARVENSE TOP | 1DP6Y6B65Z | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| WATER | 059QF0KO0R | IACT |
| SUCROSE | C151H8M554 | 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 |
|---|---|---|---|---|---|---|
| 26e2d818-afd2-9339-e063-6394a90af3f1 | b633713a-35fd-11e4-e053-2a95a90a3e1d | 2024-11-14 | Warnings | 26e2d818-afd2-9339-e063-6394a90af3f1 b633713a-35fd-11e4-e053-2a95a90a3e1d |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
