Argentum Muriaticum

Product NDC
66096-788
11-digit product format
660960788
Labeler code
66096
Product ID
66096-788_b8e2b08d-51d1-8ddb-e053-2a95a90a4357
Type
HUMAN OTC DRUG
Nonproprietary name
ARGENTUM MURIATICUM
Dosage form
PELLET
Route
ORAL
Labeler
OHM PHARMA INC.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2019-11-01
Substance
SILVER CHLORIDE
Active strength
6 [hp_C]/6[hp_C]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Reported adverse events (FAERS/openFDA)#

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

Additional Listing Data#

Finished product
Yes
Brand name base
Argentum Muriaticum
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SILVER CHLORIDE6 [hp_C]/6[hp_C]

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
MWB0804EO7Internal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
ee1b7610-8d6e-4c65-86a0-b38b8a051c4cAvailable 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
66096-788-01Argentum Muriaticum6 [hp_C] in 1 TUBEPELLET62

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
66096-788ARGENTUM MURIATICUM PELLET [OHM PHARMA INC.]2Current NDC, Legacy NDC, 1 package rows20210115_ee1b7610-8d6e-4c65-86a0-b38b8a051c4c.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
Argentum MuriaticumARGENTUM MURIATICUMOHM PHARMA INC.ee1b7610-8d6e-4c65-86a0-b38b8a051c4c2021-01-14WarningsExact identifier
ndc (product): 66096-788

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
66096-788-01660960788016 [hp_C] in 1 TUBE (66096-788-01) 2019-11-010000-00-00NoNoCurrent