FDA.reportPublic FDA data

Silver Nitrate Applicators

Product NDC
12870-0001
Requested package NDC
12870-0001-2
11-digit product format
128700001
Labeler code
12870
Product ID
12870-0001_424dba13-53c3-5abf-e063-6394a90a4722
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Silver Nitrate Applicators
Dosage form
STICK
Route
TOPICAL
Labeler
Arzol Chemical Company
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1937-01-01
Substance
POTASSIUM NITRATE; SILVER NITRATE
Active strength
25; 75 mg/100mg; mg/100mg
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 1 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopeProduct NDCPackage NDCCodeStatusReporting periodArchiveSnapshotSource SHA-256
2019-12-08 06:16 UTC · source 2019-12-05excluded packagepackage12870-000112870-0001-2EExcluded after deficient or non-compliant submission was not correctedexcluded / ndc_excluded.zip110d247fa046…a55b01930146…

Additional Listing Data#

Finished product
Yes
Brand name base
Silver Nitrate Applicators
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
POTASSIUM NITRATE25 mg/100mg
SILVER NITRATE75 mg/100mg

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
RU45X2JN0ZInternal UNII lookup
95IT3W8JZEInternal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1117536Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
23b83457-8cbc-26f1-e054-00144ff8d46cAvailable on FDA.report

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
12870-0001-1Silver Nitrate Applicators10 in 1 PACKETSTICK1013
12870-0001-1Silver Nitrate Applicators10 in 1 BOXSTICK1013
12870-0001-2Silver Nitrate Applicators100 mg in 1 APPLICATORSTICK10013
12870-0001-2Silver Nitrate Applicators100 in 1 VIALSTICK10013

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
12870-0001-1EA - Each12870-0001c2556e6d-781b-4780-bd52-6a8bd30a980a12015-12-02
12870-0001-2EA - Each12870-000135b75510-733f-4272-8c4d-8cb80209abd512015-12-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
SILVER NITRATEACTIVE INGREDIENT95IT3W8JZESILVER NITRATE APPLICATORS STICK [ARZOL CHEMICAL COMPANY]4
SILVER CATIONACTIVE MOIETY57N7B0K90ASILVER NITRATE APPLICATORS STICK [ARZOL CHEMICAL COMPANY]4
POTASSIUM NITRATEINACTIVE INGREDIENTRU45X2JN0ZSILVER NITRATE APPLICATORS STICK [ARZOL CHEMICAL COMPANY]4

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
12870-0001SILVER NITRATE APPLICATORS STICK [ARZOL CHEMICAL COMPANY]12Current NDC, Legacy NDC, 4 package rows20241012_23b83457-8cbc-26f1-e054-00144ff8d46c.zip

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
Silver Nitrate ApplicatorsSILVER NITRATE APPLICATORSArzol Chemical Company23b83457-8cbc-26f1-e054-00144ff8d46c2025-10-29Warnings, Adverse reactionsExact identifier
ndc (package): 12870-0001-2
ndc (product): 12870-0001
ndc11 (package): 12870000102

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1117536potassium nitrate 25 % / silver nitrate 75 % Medicated PadPSN23b83457-8cbc-26f1-e054-00144ff8d46c13
1117536potassium nitrate 250 MG/ML / silver nitrate 750 MG/ML Medicated PadSCD23b83457-8cbc-26f1-e054-00144ff8d46c13
1117536K+ nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY23b83457-8cbc-26f1-e054-00144ff8d46c13
1117536Pot nitrate 250 MG/ML / AgNO3 750 MG/ML Medicated PadSY23b83457-8cbc-26f1-e054-00144ff8d46c13
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SpongeSY23b83457-8cbc-26f1-e054-00144ff8d46c13
1117536potassium nitrate 25 % / silver nitrate 75 % Topical StickSY23b83457-8cbc-26f1-e054-00144ff8d46c13
1117536potassium nitrate 25 % / silver nitrate 75 % Topical SwabSY23b83457-8cbc-26f1-e054-00144ff8d46c13

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
12870-0001-212870000102100 APPLICATOR in 1 VIAL (12870-0001-2) / 100 mg in 1 APPLICATOR100 applicator1937-01-010000-00-00NoNoCurrent