Prunus spinosa e summ 10%

Product NDC
48951-8082
11-digit product format
489518082
Labeler code
48951
Product ID
48951-8082_6b139bac-888f-4b86-e053-2991aa0a5cbe
Type
HUMAN OTC DRUG
Nonproprietary name
Prunus spinosa e summ 10%
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
PRUNUS SPINOSA WHOLE
Active strength
10 g/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8082-3Prunus spinosa e summ 10%1 in 1 BOTTLE, GLASSLIQUID13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
PRUNUS SPINOSA WHOLEACTIVE INGREDIENT5342MY2M3PPRUNUS SPINOSA E SUMM 10% LIQUID [URIEL PHARMACY INC.]1
PRUNUS SPINOSA WHOLEACTIVE MOIETY5342MY2M3PPRUNUS SPINOSA E SUMM 10% LIQUID [URIEL PHARMACY INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MPRUNUS SPINOSA E SUMM 10% LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RPRUNUS SPINOSA E SUMM 10% LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8082PRUNUS SPINOSA E SUMM 10% LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 1 package rows20180430_80c115e6-049e-4e12-a0e9-78d484b57bae.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8082-3489518082031 LIQUID in 1 BOTTLE, GLASS (48951-8082-3) 1 liquid2009-09-010000-00-00NoNoCurrent