Viscum Crataegi Series 1

Product NDC
48951-9207
11-digit product format
489519207
Labeler code
48951
Product ID
48951-9207_6bdfa456-d5a0-2ccd-e053-2a91aa0a1a82
Type
HUMAN OTC DRUG
Nonproprietary name
Viscum Crataegi Series 1
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
6 [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
48951-9207-1Viscum Crataegi Series 110 in 1 PACKAGE, COMBINATIONLIQUID104
48951-9207-1Viscum Crataegi Series 11 mL in 1 AMPULELIQUID14

DailyMed Socrata Ingredients#

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

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9207VISCUM CRATAEGI SERIES 1 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20231230_7f679f06-d795-4a61-9f18-4bba60943943.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9207-14895192070110 AMPULE in 1 PACKAGE, COMBINATION (48951-9207-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent