Cactus Cinis Avenae
- Manufacturer
- Uriel Pharmacy Inc.
- Effective date
- 2020-12-18
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- full-release
- Hydrated at
- 2026-06-01 02:14:02
Label at a glance#
Contacts and useful links#
Label 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 Ingredients: Cactus (Queen of the night) 3X, Crataegus (Hawthorn) 3X,Magnesium phos. e cin. Avenae (Magnesium phosphate in ash of oat grains) 6X, Arnica 20X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt, Lactose
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. Contains traces of lactose. 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
Made by Uriel, East Troy, WI 53120
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 48951-3239-1 | Cactus Cinis Avenae | 10 in 1 BOX | LIQUID | 10 | 1 | |
| 48951-3239-1 | Cactus Cinis Avenae | 1 mL in 1 AMPULE | LIQUID | 1 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-3239 | CACTUS CINIS AVENAE LIQUID [URIEL PHARMACY INC.] | 1 | Legacy NDC, 2 package rows | 20201219_b6c13079-0ecf-0d79-e053-2a95a90a8d7c.zip |
Products#
Every source-derived product name is available through these pages.
- Cactus Cinis Avenae
- LACTOSE, UNSPECIFIED FORM
- MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE
- MAGNESIUM CATION
- SELENICEREUS GRANDIFLORUS STEM
- HAWTHORN LEAF WITH FLOWER
- SODIUM CHLORIDE
- ARNICA MONTANA FLOWER
- WATER
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-3239 | 48951-3239-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | IACT |
| MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE | 453COF7817 | ACTIB |
| SELENICEREUS GRANDIFLORUS STEM | 7114SV0MYK | ACTIB |
| HAWTHORN LEAF WITH FLOWER | 6OM09RPY36 | ACTIB |
| SODIUM CHLORIDE | 451W47IQ8X | IACT |
| ARNICA MONTANA FLOWER | OZ0E5Y15PZ | ACTIB |
| WATER | 059QF0KO0R | 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 |
|---|---|---|---|---|---|---|
| b6c13079-0ed0-0d79-e053-2a95a90a8d7c | b6c13079-0ecf-0d79-e053-2a95a90a8d7c | 2020-12-18 | Warnings | b6c13079-0ed0-0d79-e053-2a95a90a8d7c b6c13079-0ecf-0d79-e053-2a95a90a8d7c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
