Silver Nitrate

Manufacturer
Gordon Laboratories
Effective date
2015-07-28
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
8
Source
legacy-cache
Hydrated at
2026-08-02 01:31:03

Label at a glance#

ProductSilver Nitrate
Active ingredientSILVER NITRATE
Label structure6 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Silver Nitrate Solution 50 percent, Purifed  water

HOW SUPPLIED SECTION

Silver Nitrate Solution Fifty Percent is supplied in a 1 oz. Amber Glass Bottle.

SPL UNCLASSIFIED SECTION

Silver Nitrate Solution 50%, Purified water

INDICATIONS & USAGE SECTION

Strong escharotic, dehydrating and sclerosing agent.

WARNINGS AND PRECAUTIONS SECTION

Do not apply to wounds, cuts or broken skin.  Prolonged or frequent use may result in a permanent discoloration of the skin. Federal law prohibits dispensing without a prescription. For physician use only. Keep out of reach of children. For external use only. Harmful if taken internally. If swallowed, do not induce vomiting. Give large quantities of water. Never give anything by mouth to an unconscious person. If inhaled, remove to fresh air. In case of contact, immediately flush eyes or skin with plenty of water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse. In all cases get medical attention immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Silver Nitrate Solution 50%Image of Silver Nitrate Solution 50%

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10481-1053-12021-11-03C16284748780-19d75b9d0-f6a9-f424-e053-dadaa90a57ceSilver Nitrate
10481-1053-12020-01-31C16284748780-19d75b9d0-f6a9-f424-e053-dadaa90a57ceSilver Nitrate

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10481-1053-1ML - Milliliter10481-10532626adcb-ee94-4df3-92e5-0970367118fc12013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE8
SILVER CATIONACTIVE MOIETY57N7B0K90A8
WATERINACTIVE INGREDIENT059QF0KO0R8

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
10481-105310481-1053-1

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
cfe4dae3-9a6a-5424-e053-2995a90a99447038f51e-0749-4142-bbcd-2eab6638438e2021-11-03WarningsExact identifier
spl set id: 7038f51e-0749-4142-bbcd-2eab6638438e

Reported adverse events (FAERS/openFDA)#

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