FDA.reportPublic FDA data

Silver Nitrate

Manufacturer
Gordon Laboratories
Effective date
2015-07-30
Label type
HUMAN PRESCRIPTION DRUG LABEL
Version
5
Source
legacy-cache
Hydrated at
2026-08-02 01:31:02

Label at a glance#

ProductSilver Nitrate
Active ingredientSILVER NITRATE
Label structure7 sections

Label contents#

Full prescribing information#

DESCRIPTION SECTION

Silver Nitrate Solution is a colorless, odorless, transparent solution used as an escharotic, dehydrating and sclerosing agent.

HOW SUPPLIED SECTION

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

SPL UNCLASSIFIED SECTION

Silver Nitrate 25% Solution, Purified water

INDICATIONS & USAGE SECTION

Escharotic, dehydrating and sclerosing agent.

WARNINGS AND PRECAUTIONS SECTION

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 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.

SPL UNCLASSIFIED SECTION

Store at room temperature 59-86F(15-30C).

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of Silver Nitrate Solution 25% Label
Image of Silver Nitrate Solution 25% Label

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850217001839GTIN-13: 0850217001839
EAN-13: 0850217001839
GTIN-12: 850217001839
UPC-A: 850217001839
GTIN storage (14 digits): 00850217001839		sns25.jpg

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10481-1052-12021-11-03C16284748780-19d75b9d0-ca0c-f424-e053-dadaa90a57ceSILVER NITRATE
10481-1052-12020-01-31C16284748780-19d75b9d0-ca0c-f424-e053-dadaa90a57ceSILVER NITRATE

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10481-1052-1ML - Milliliter10481-105283a8b9ce-ed62-44e3-b6ec-edb077d3b78312013-02-13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZE5
SILVER CATIONACTIVE MOIETY57N7B0K90A5
WATERINACTIVE INGREDIENT059QF0KO0R5

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
10481-105210481-1052-1

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
cfe3a96c-6b75-19cf-e053-2a95a90acf8840cd0087-6537-4451-9d1c-cbaf6d5969252021-11-03WarningsExact identifier
spl set id: 40cd0087-6537-4451-9d1c-cbaf6d596925

Reported adverse events (FAERS/openFDA)#

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