Ferrum arsenicosum 6

Product NDC
48951-4057
11-digit product format
489514057
Labeler code
48951
Product ID
48951-4057_6ab14206-d66d-441a-e053-2a91aa0a0052
Type
HUMAN OTC DRUG
Nonproprietary name
Ferrum arsenicosum 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
FERROUS ARSENATE
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
48951-4057-1Ferrum arsenicosum 61 mL in 1 AMPULELIQUID13
48951-4057-1Ferrum arsenicosum 610 in 1 BOXLIQUID103

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
FERROUS ARSENATEACTIVE INGREDIENT129CO35H12FERRUM ARSENICOSUM 6 LIQUID [URIEL PHARMACY INC.]1
FERROUS ARSENATEACTIVE MOIETY129CO35H12FERRUM ARSENICOSUM 6 LIQUID [URIEL PHARMACY INC.]1
LACTOSEINACTIVE INGREDIENTJ2B2A4N98GFERRUM ARSENICOSUM 6 LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XFERRUM ARSENICOSUM 6 LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RFERRUM ARSENICOSUM 6 LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4057FERRUM ARSENICOSUM 6 LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20180425_83965984-298f-4944-a654-acc709286ec1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4057-14895140570110 AMPULE in 1 BOX (48951-4057-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent