FDA.reportPublic FDA data

Germproof

Product NDC
72363-006
Requested package NDC
72363-006-03
11-digit product format
723630006
Labeler code
72363
Product ID
72363-006_4cd740ed-ae62-9c89-e063-6394a90aa9a3
Type
HUMAN OTC DRUG
Nonproprietary name
Argentum Metallicum
Dosage form
GEL
Route
TOPICAL
Labeler
AG Essence
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2022-03-14
Substance
SILVER
Active strength
1 g/28.5g
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage72363-00672363-006-03DDiscontinued by firm2026-08-11

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 · 5 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source dateSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-312ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21cfe11265f3b6…090c488252e2…

Additional Listing Data#

Finished product
Yes
Brand name base
Germproof
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILVER1 g/28.5g

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
3M4G523W1GInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
d9e2cfe3-a65d-2637-e053-2a95a90afc56Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
72363-006-02Germproof28.5 g in 1 BOTTLE, SPRAYGEL28.53
72363-006-03Germproof1 in 1 BOXGEL13

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
GermproofARGENTUM METALLICUMAG Essenced9e2cfe3-a65d-2637-e053-2a95a90afc562026-03-12WarningsExact identifier
ndc (package): 72363-006-03
ndc (product): 72363-006
ndc11 (package): 72363000603

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
72363-006-03723630006031 BOTTLE, SPRAY in 1 BOX (72363-006-03) > 28.5 g in 1 BOTTLE, SPRAY (72363-006-02) 2022-03-142025-03-14NoNoCurrent