Hamamelis e cortex 3

Product NDC
48951-5030
11-digit product format
489515030
Labeler code
48951
Product ID
48951-5030_8ea24680-6d7d-4bb7-8f42-21ed2c577491
Type
HUMAN OTC DRUG
Nonproprietary name
Hamamelis e cortex 3
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
HAMAMELIS VIRGINIANA TOP
Active strength
3 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
fb7ab793-2c12-4079-b100-a64f73bef25aProduct name420240712
b0cbf770-6cc3-4aa4-9158-755110c2b9f7Product name220230717
dc7c5daa-021f-40dd-b00d-63982cb2067aProduct name120230426
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name520200925
816b97af-edc5-4060-aff1-b814bdbcad50Product name120190415
7cda52fc-125f-421c-8fea-bc1974370c49Product name220180703
419aab54-5d5a-4146-9453-026d4a9991beProduct name220170525
08ffbcbf-26df-b99c-1dab-64fc4cfae89fProduct name220160823
89dac932-b90a-4410-9ab1-84c53e57de25Product name120150316

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-5030-12020-01-31C16284748780-19d75b9d0-4783-f424-e053-dadaa90a57ceHamamelis e cortex 3

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-5030-1Hamamelis e cortex 37 mL in 1 BOTTLE, DROPPERLIQUID71
48951-5030-1Hamamelis e cortex 31 in 1 BAGLIQUID11

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
HAMAMELIS VIRGINIANA TOPACTIVE INGREDIENTUDA30A2JJYHAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1
HAMAMELIS VIRGINIANA TOPACTIVE MOIETYUDA30A2JJYHAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1
ROSE OILINACTIVE INGREDIENTWUB68Y35M7HAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1
SODIUM BICARBONATEINACTIVE INGREDIENT8MDF5V39QOHAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XHAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RHAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-5030HAMAMELIS E CORTEX 3 LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20140909_631fc5b9-55f0-4a6a-8488-afbfd3073e60.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
48951-5030-1489515030017 mL in 1 BOTTLE, DROPPER7 mlHistorical