Argentum nitricum
- Manufacturer
- Boiron | Boiron, Inc.
- Effective date
- 2025-09-23
- Label type
- HUMAN OTC DRUG LABEL
- Version
- 4
- Source
- full-release
- Hydrated at
- 2026-06-01 02:35:06
Label at a glance#
Contacts and useful links#
Label contents#
Full prescribing information#
OTC - ACTIVE INGREDIENT SECTION
Active ingredient** (in each pellet)
Argentum nitricum 30C HPUS (0.44 mg)
(contains less than 10 -12 mg silver)
The letters “HPUS” indicate that the component in this product is officially monographed in the Homeopathic Pharmacopoeia of the United States.
OTC - PURPOSE SECTION
Purpose*
Argentum nitricum 30C HPUS (0.44 mg)…………….…Relieves apprehension with heartburn
INDICATIONS & USAGE SECTION
Uses*
temporarily relieves symptoms of occasional stress such as:
▪ nervousness ▪ apprehension ▪ stage fright ▪ heartburn caused by stress
OTC - STOP USE SECTION
Stop use and ask a doctor if symptoms persist for more than 3 days or worsen. If you have trouble swallowing or persistent abdominal pain, see your doctor promptly.
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. In case of overdose, get medical help or contact a Poison Control Center right away.
DOSAGE & ADMINISTRATION SECTION
- Adults and children 12 years of age and older: At the onset of symptoms, dissolve 5 pellets under the tongue 3 times a day until symptoms are relieved or as directed by a doctor.
- Children under 12 years of age: Ask a doctor.
INACTIVE INGREDIENT SECTION
lactose, sucrose
OTC - QUESTIONS SECTION
BoironUSA.com
Info@Boiron.com
1-800-BOIRON-1 (1-800-264-7661)
Made in France
Distributed by Boiron Inc.
Newtown Square, PA 19073
SPL UNCLASSIFIED SECTION
- do not use if glued carton end flaps are open or if pellet dispenser seal is broken
- contains 0.25 g of sugar per dose
- retain carton for full drug facts
3 TUBES
APPROX. 80 PELLETS EACH
TOTAL 240 PELLETS
16 DOSES PER TUBE
STRESS RELIEF*
Do not use if pellet dispenser seal is broken.
Contains approx 80 pellets.
How to dispense pellets? Turn tube upside down. Twist until 5 pellets are dispensed into cap. Carefully remove the cap and use it to pour pellets under the tongue.
*CLAIMS BASED ON TRADITIONAL HOMEOPATHIC PRACTICE NOT ACCEPTED MEDICAL EVIDENCE. NOT FDA EVALUATED.
*C,K,CK, and X are homeopathic dilutions: see BoironUSA.com/info for details.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| 6cca4355-1206-91f7-02de-17eef38a8622 | Product name | 1 | 20140508 |
| 751c581a-bf64-2fd7-b3ec-ca02c83e4a00 | Product name | 1 | 20140508 |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0220-0465-41 | Argentum nitricum | 30 [hp_C] in 1 TUBE | PELLET | 30 | 4 | |
| 0220-0465-43 | Argentum nitricum | 3 in 1 BOX | PELLET | 3 | 4 |
Products#
Every source-derived product name is available through these pages.
- Argentum nitricum
- SILVER NITRATE
- SUCROSE
- SILVER CATION
- LACTOSE, UNSPECIFIED FORM
- ANHYDROUS LACTOSE
NDC Codes#
| Product NDC | Package NDC |
|---|---|
| 0220-0465 | 0220-0465-41, 0220-0465-43 |
Ingredients#
Every source-derived ingredient row is available through these pages.
| Name | UNII | Kind |
|---|---|---|
| SUCROSE | C151H8M554 | IACT |
| SILVER NITRATE | 95IT3W8JZE | ACTIB |
| LACTOSE, UNSPECIFIED FORM | J2B2A4N98G | 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 |
|---|---|---|---|---|---|---|
| Argentum nitricum | SILVER NITRATE | Boiron | 8461ee54-31ee-1af2-e053-2a91aa0ad9e3 | 2025-09-23 | 0220-0465-43 0220-0465-41 0220-0465 00220046541 00220046543 3f7a8a3b-cddd-0c6d-e063-6294a90a69ea 8461ee54-31ee-1af2-e053-2a91aa0ad9e3 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.



