Calendula 3 Special Order
- Manufacturer
- Uriel Pharmacy, Inc.
- Effective date
- 2019-02-12
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-02 00:31:12
Label at a glance#
ProductCalendula 3 Special Order
Active ingredientCALENDULA OFFICINALIS FLOWERING TOP
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 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: Calendula 3X
INACTIVE INGREDIENT SECTION
Inactive Ingredients: Water, Salt, Boric acid, Sodium bicarbonate, Rose oil
OTC - PURPOSE SECTION
Use: Promotes healing of cuts, grazes and wounds.
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
www.urielpharmacy.com
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Calendula 3 Special Order
- WATER
- ROSE OIL
- CALENDULA OFFICINALIS FLOWERING TOP
- BORIC ACID
- SODIUM BICARBONATE
- SODIUM CHLORIDE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 48951-3227 | 48951-3227-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| WATER | 059QF0KO0R | IACT |
| ROSE OIL | WUB68Y35M7 | IACT |
| CALENDULA OFFICINALIS FLOWERING TOP | 18E7415PXQ | ACTIB |
| BORIC ACID | R57ZHV85D4 | IACT |
| SODIUM BICARBONATE | 8MDF5V39QO | IACT |
| SODIUM CHLORIDE | 451W47IQ8X | 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 |
|---|---|---|---|---|---|---|
| c707094f-c5fd-da64-e053-2995a90a1ff2 | 81b8aae5-a4d9-e89d-e053-2a91aa0a3072 | 2021-07-13 | Warnings | 81b8aae5-a4d9-e89d-e053-2a91aa0a3072 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.