Dosage and administration
(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.
Argentum Nitricum
- Manufacturer
- SEVENE USA
- Effective date
- 2022-06-10
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 1
- Source
- legacy-cache
- Hydrated at
- 2026-08-01 21:59:27
Label at a glance#
ProductArgentum Nitricum
Active ingredientSILVER NITRATE
Label structure13 sections
Contacts and useful links#
Websitewww.ollois.com
www.ollois.com
www.ollois.comLabel contents#
Full prescribing information#
ACTIVE INGREDIENT
HOMEOPATHIC DILUTION OF HPUS Argentum Nitricum 6c.
TRADITIONALLY USED FOR
Nervous anticipation with occasional heartburn* - Stage fright*
DIRECTIONS
(adults/children) Dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a physician.
USE
Condition listed above or as directed by a physician.
WARNINGS
Stop use and ask a physician if symptoms persist for more than 3 days or worsen.
OTC - PREGNANCY OR BREAST FEEDING SECTION
If pregnant or breast-feeding, ask a health professional before use.
OTC - KEEP OUT OF REACH OF CHILDREN SECTION
Keep out of reach of children.
OTHER INFORMATION
Store at room temperature.
OTC - DO NOT USE SECTION
Do not use if pellet-dispenser seal is broken.
INACTIVE INGREDIENT
Sucrose.
QUESTIONS?
INFO@OLLOIS.COM * www.ollois.com * MADE IN FRANCE. NOT REVIEWED BY THE FDA AND NOT GUARANTEED TO BE EFFECTIVE. THIS HOMEOPATHIC DILUTION MAY NOT BE SUSEPTIBLE TO SCIENTIFIC MEASUREMENT.
USE:
Condition listed above or as directed by a physician.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
Products#
Every source-derived product name is available through these pages.
- Argentum Nitricum
- SILVER NITRATE
- SUCROSE
- SILVER CATION
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 76472-4003 | 76472-4003-1 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| SILVER NITRATE | 95IT3W8JZE | 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 |
|---|---|---|---|---|---|---|
| 05418455-0140-71ff-e063-6294a90a0c94 | e11da315-d709-7b80-e053-2995a90a1ba7 | 2023-09-13 | Warnings | e11da315-d709-7b80-e053-2995a90a1ba7 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.