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#

ProductArgentum nitricum
Active ingredientSILVER NITRATE
Label structure11 sections

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

09250925

09250925

0925092509250925

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
6cca4355-1206-91f7-02de-17eef38a8622Product name120140508
751c581a-bf64-2fd7-b3ec-ca02c83e4a00Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0220-0465-41Argentum nitricum30 [hp_C] in 1 TUBEPELLET304
0220-0465-43Argentum nitricum3 in 1 BOXPELLET34

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0220-04650220-0465-41, 0220-0465-43

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 3 matching rows.

Source Document#

Source XML

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.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Argentum nitricumSILVER NITRATEBoiron8461ee54-31ee-1af2-e053-2a91aa0ad9e32025-09-23Exact identifier
ndc (package): 0220-0465-43
ndc (package): 0220-0465-41
ndc (product): 0220-0465
ndc11 (package): 00220046541
ndc11 (package): 00220046543
spl id: 3f7a8a3b-cddd-0c6d-e063-6294a90a69ea
spl set id: 8461ee54-31ee-1af2-e053-2a91aa0ad9e3

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.