Thymus Mercurius

Product NDC
48951-9008
11-digit product format
489519008
Labeler code
48951
Product ID
48951-9008_4484b0ab-6d8e-870b-e063-6294a90af92d
Type
HUMAN OTC DRUG
Nonproprietary name
Thymus Mercurius
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
BOS TAURUS THYMUS; MERCURY
Active strength
8; 20 [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Thymus Mercurius
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
BOS TAURUS THYMUS8 [hp_X]/mL
MERCURY20 [hp_X]/mL

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
8XEJ88V2T8Internal UNII lookup
FXS1BY2PGLInternal UNII lookup

Harmonized SPL set identifiers#

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

Identifier, FDA.report destination table
IdentifierFDA.report destination
28c34cbd-a0c2-4b6a-a923-acbfd75c840cAvailable on FDA.report

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9008-1Thymus Mercurius1 mL in 1 AMPULELIQUID14
48951-9008-1Thymus Mercurius10 in 1 BOXLIQUID104

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
BOS TAURUS THYMUSACTIVE INGREDIENT8XEJ88V2T8THYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]1
MERCURYACTIVE INGREDIENTFXS1BY2PGLTHYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]1
BOS TAURUS THYMUSACTIVE MOIETY8XEJ88V2T8THYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]1
MERCURYACTIVE MOIETYFXS1BY2PGLTHYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XTHYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RTHYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9008THYMUS MERCURIUS LIQUID [URIEL PHARMACY INC.]3Current NDC, Legacy NDC, 2 package rows20231123_28c34cbd-a0c2-4b6a-a923-acbfd75c840c.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
Thymus MercuriusTHYMUS MERCURIUSUriel Pharmacy Inc.28c34cbd-a0c2-4b6a-a923-acbfd75c840c2025-11-26WarningsExact identifier
ndc (product): 48951-9008

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9008-14895190080110 AMPULE in 1 BOX (48951-9008-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent