SILVER NITRATE SOLUTION

Manufacturer
Gordon Laboratories
Effective date
2015-07-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
4
Source
legacy-cache
Hydrated at
2026-08-02 01:31:01

Label at a glance#

ProductSilver Nitrate
Active ingredientSILVER NITRATE
Label structure8 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Silver Nitrate 10%, Purified water

HOW SUPPLIED SECTION

Silver Nitrate Solution 10% is supplied as 1 oz Amber Glass Bottle






SPL UNCLASSIFIED SECTION


Silver Nitrate 10%, Purified water

INDICATIONS & USAGE SECTION

Epithelial stimulant, astrigent,and germicidal action, treatment of helomas.

Apply to area or lesion with a cotton applicator dipped in solution, two or three times weekly for two or three weeks as needed.

WARNINGS AND PRECAUTIONS SECTION

Do not apply to wounds,cuts or broken skin. Prolonged or frequent use may result in permanent discoloration of the skin.

Keep out of reach of children. For external use only. Harmful if taken internally. If swallowed , do not induce vomiting.

In case of contact immediately flush eyes or skin with plenty of water for ateleast 15 minutes.

SPL UNCLASSIFIED SECTION

Federal law prohibits dispensing without prescription. Physician use only.

SPL UNCLASSIFIED SECTION

Store at room temperature 59 o-86 oF (15 o-30 oC)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Silver Nitrate Solution Label
Image of Silver Nitrate Solution Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850217001822GTIN-13: 0850217001822
EAN-13: 0850217001822
GTIN-12: 850217001822
UPC-A: 850217001822
GTIN storage (14 digits): 00850217001822
sns10.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10481-1051-12021-11-03C16284748780-19d75b9d0-7243-f424-e053-dadaa90a57ceSILVER NITRATE SOLUTION
10481-1051-12020-01-31C16284748780-19d75b9d0-7243-f424-e053-dadaa90a57ceSILVER NITRATE SOLUTION

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10481-1051-1ML - Milliliter10481-10515f05b82c-8d49-4f2f-93a5-cf26c7e7122312012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE4
SILVER CATIONACTIVE MOIETY57N7B0K90A4
WATERINACTIVE INGREDIENT059QF0KO0R4

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
10481-105110481-1051-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SILVER NITRATE95IT3W8JZEACTIB

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
cfd523cf-9e42-f912-e053-2a95a90a4cbb2c5c94b7-aa51-4764-b3af-184d74c8eaaf2021-11-02WarningsExact identifier
spl set id: 2c5c94b7-aa51-4764-b3af-184d74c8eaaf

Reported adverse events (FAERS/openFDA)#

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