Cuprum sulfuricum 6

Product NDC
48951-3146
11-digit product format
489513146
Labeler code
48951
Product ID
48951-3146_6aaeab59-d842-a66c-e053-2a91aa0a71ec
Type
HUMAN OTC DRUG
Nonproprietary name
Cuprum sulfuricum 6
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CUPRIC SULFATE
Active strength
6 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
0306390c-dd77-4363-afe0-63c58088b2a1Product name120220120
503ea967-4b9c-48cf-9e87-c7975295849dProduct name220220120

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3146-3Cuprum sulfuricum 660 mL in 1 BOTTLE, DROPPERLIQUID604

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
CUPRIC SULFATEACTIVE INGREDIENTLRX7AJ16DTCUPRUM SULFURICUM 6 LIQUID [URIEL PHARMACY INC.]1
CUPRIC CATIONACTIVE MOIETY8CBV67279LCUPRUM SULFURICUM 6 LIQUID [URIEL PHARMACY INC.]1
ALCOHOLINACTIVE INGREDIENT3K9958V90MCUPRUM SULFURICUM 6 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RCUPRUM SULFURICUM 6 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3146CUPRUM SULFURICUM 6 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 1 package rows20241210_b240d55e-0daf-425a-83c1-93da5a65cd17.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3146-34895131460360 mL in 1 BOTTLE, DROPPER (48951-3146-3) 60 ml2009-09-010000-00-00NoNoCurrent