Viscum Crataegi

Product NDC
48951-1002
11-digit product format
489511002
Labeler code
48951
Product ID
48951-1002_6bdf230e-99f4-cada-e053-2a91aa0a0c8a
Type
HUMAN OTC DRUG
Nonproprietary name
VISCUM ALBUM FRUITING TOP
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
48951-1002-1Viscum Crataegi1 mL in 1 AMPULELIQUID13
48951-1002-1Viscum Crataegi10 in 1 PACKAGELIQUID103

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
VISCUM ALBUM FRUITING TOPACTIVE INGREDIENTBK9092J5MPVISCUM CRATAEGI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]1
VISCUM ALBUM FRUITING TOPACTIVE MOIETYBK9092J5MPVISCUM CRATAEGI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]1
Sodium ChlorideINACTIVE INGREDIENT451W47IQ8XVISCUM CRATAEGI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]1
WaterINACTIVE INGREDIENT059QF0KO0RVISCUM CRATAEGI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-1002VISCUM CRATAEGI (VISCUM ALBUM FRUITING TOP) LIQUID [URIEL PHARMACY INC]3Legacy NDC, 2 package rows20180514_39aa8b8e-26b6-49c7-9259-5a00d6525fa6.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-1002-14895110020110 AMPULE in 1 PACKAGE (48951-1002-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent