Quercus Cinis

Product NDC
48951-8117
11-digit product format
489518117
Labeler code
48951
Product ID
48951-8117_6b15706b-197d-beba-e053-2991aa0a1734
Type
HUMAN OTC DRUG
Nonproprietary name
Quercus Cinis
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
QUERCUS ROBUR WHOLE
Active strength
5 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
IngredientStrength
QUERCUS ROBUR WHOLE5 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiR7QMG0BT2W

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8117-1Quercus Cinis10 in 1 BOXLIQUID105
48951-8117-1Quercus Cinis1 mL in 1 AMPULELIQUID15

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
QUERCUS ROBUR WHOLEACTIVE INGREDIENTR7QMG0BT2WQUERCUS CINIS LIQUID [URIEL PHARMACY INC.]1
QUERCUS ROBUR WHOLEACTIVE MOIETYR7QMG0BT2WQUERCUS CINIS LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XQUERCUS CINIS LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RQUERCUS CINIS LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8117QUERCUS CINIS LIQUID [URIEL PHARMACY INC.]5Legacy NDC, 2 package rows20241206_40f9a50c-0d41-43c3-b3a0-d564eca811b3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8117-14895181170110 AMPULE in 1 BOX (48951-8117-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent