Chamomilla Cupro 3X
- Manufacturer
- Uriel Pharmacy, Inc.
- Effective date
- 2024-11-14
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 20:49:18
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: Chamomilla Cupro (Chamomile) 3X
INACTIVE INGREDIENT SECTION
Inactive Ingredient: Distilled water, 20% Organic cane alcohol
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. 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 Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 48951-3272 | CHAMOMILLA CUPRO 3X LIQUID [URIEL PHARMACY, INC.] | 1 | Unmatched | 20241116_26e46565-da4e-148a-e063-6394a90ac19c.zip |
Products#
Every source-derived product name is available through these pages.
- Chamomilla Cupro 3X
- ALCOHOL
- WATER
- MATRICARIA CHAMOMILLA
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-3272 | 48951-3272-3 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| ALCOHOL | 3K9958V90M | IACT |
| WATER | 059QF0KO0R | IACT |
| MATRICARIA CHAMOMILLA | G0R4UBI2ZZ | 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 |
|---|---|---|---|---|---|---|
| 4d7af5c6-8b7b-154e-e063-6294a90a3583 | 26e46565-da4e-148a-e063-6394a90ac19c | 2026-03-20 | Warnings | 26e46565-da4e-148a-e063-6394a90ac19c |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
