Viscum Tiliae Series 2

Product NDC
48951-9220
11-digit product format
489519220
Labeler code
48951
Product ID
48951-9220_6c2bdcb4-6f3d-bebd-e053-2a91aa0ad09c
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Tiliae Series 2
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
VISCUM ALBUM FRUITING TOP
Active strength
2 [hp_X]/mL
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
48951-9220-1Viscum Tiliae Series 21 mL in 1 AMPULELIQUID16
48951-9220-1Viscum Tiliae Series 210 in 1 BOXLIQUID106

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM TILIAE SERIES 2 LIQUID [URIEL PHARMACY INC.]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM TILIAE SERIES 2 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XVISCUM TILIAE SERIES 2 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RVISCUM TILIAE SERIES 2 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9220VISCUM TILIAE SERIES 2 LIQUID [URIEL PHARMACY INC.]6Legacy NDC, 2 package rows20241208_6dabd8ca-20eb-4b2d-a59c-a4ca70babfac.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9220-14895192200110 AMPULE in 1 BOX (48951-9220-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent