Cinnabar Dandelion

Product NDC
48951-3101
11-digit product format
489513101
Labeler code
48951
Product ID
48951-3101_6c54d80c-209f-f21d-e053-2991aa0aa023
Type
HUMAN OTC DRUG
Nonproprietary name
Cinnabar Dandelion
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
ELYMUS REPENS ROOT; TARAXACUM PALUSTRE ROOT; FERROUS DISULFIDE; CARBONATE ION; MERCURIC CATION
Active strength
3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-3101DDiscontinued by firm2026-10-05
excluded packagepackage48951-310148951-3101-1DDiscontinued by firm2026-10-05

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 · 18 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source dateDatasetScopePackage NDCSnapshotSource SHA-256
2025-12-14 17:58 UTC · source 2025-12-05excluded productproductd630ba8d3edf…732f749b63fb…
2025-12-14 17:58 UTC · source 2025-12-05excluded packagepackage48951-3101-1d630ba8d3edf…732f749b63fb…
2025-08-27 00:01 UTC · source 2025-08-26excluded productproductf5e01cc5f278…a2eaf40c39c3…
2025-08-27 00:01 UTC · source 2025-08-26excluded packagepackage48951-3101-1f5e01cc5f278…a2eaf40c39c3…
2025-04-01 02:39 UTC · source 2025-03-31excluded productproduct2ef7874e63bc…57b86245f4fa…
2025-04-01 02:39 UTC · source 2025-03-31excluded packagepackage48951-3101-12ef7874e63bc…57b86245f4fa…
2025-03-28 20:22 UTC · source 2025-03-28excluded productproducta1b67e2a42f9…c4cf2c586c0d…
2025-03-28 20:22 UTC · source 2025-03-28excluded packagepackage48951-3101-1a1b67e2a42f9…c4cf2c586c0d…
2025-03-22 03:12 UTC · source 2025-03-21excluded productproductcfe11265f3b6…090c488252e2…
2025-03-22 03:12 UTC · source 2025-03-21excluded packagepackage48951-3101-1cfe11265f3b6…090c488252e2…
2025-03-10 12:48 UTC · source 2025-03-10excluded productproductcdf11ea48f46…ba0047e9e063…
2025-03-10 12:48 UTC · source 2025-03-10excluded packagepackage48951-3101-1cdf11ea48f46…ba0047e9e063…
2025-02-02 03:52 UTC · source 2025-01-31excluded productproduct302b2466d912…e7b80fea0513…
2025-02-02 03:52 UTC · source 2025-01-31excluded packagepackage48951-3101-1302b2466d912…e7b80fea0513…
2025-01-20 13:05 UTC · source 2025-01-20excluded productproducted331223b511…672a5bd82f5f…
2025-01-20 13:05 UTC · source 2025-01-20excluded packagepackage48951-3101-1ed331223b511…672a5bd82f5f…
2025-01-11 03:41 UTC · source 2025-01-10excluded productproduct0efc9e666f02…f202fb6c5f17…
2025-01-11 03:41 UTC · source 2025-01-10excluded packagepackage48951-3101-10efc9e666f02…f202fb6c5f17…

Reported adverse events (FAERS/openFDA)#

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

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CARBONATE IONACTIVE INGREDIENT7UJQ5OPE7DCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
ELYMUS REPENS ROOTACTIVE INGREDIENT3IXW0F6P8WCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
FERROUS DISULFIDEACTIVE INGREDIENT132N09W4PRCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
MERCURIC CATIONACTIVE INGREDIENTED30FJ8Y42CINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
TARAXACUM PALUSTRE ROOTACTIVE INGREDIENTGCZ4W7077CCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
CARBONATE IONACTIVE MOIETY7UJQ5OPE7DCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
ELYMUS REPENS ROOTACTIVE MOIETY3IXW0F6P8WCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
FERROUS CATIONACTIVE MOIETYGW89581OWRCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
MERCURIC CATIONACTIVE MOIETYED30FJ8Y42CINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
TARAXACUM PALUSTRE ROOTACTIVE MOIETYGCZ4W7077CCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCINNABAR DANDELION LIQUID [URIEL PHARMACY INC.]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3101-14895131010110 AMPULE in 1 BOX (48951-3101-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent