Rhus Aconitum

Product NDC
48951-8140
11-digit product format
489518140
Labeler code
48951
Product ID
48951-8140_4bd37192-f7e8-b961-e063-6294a90ab3d3
Type
HUMAN OTC DRUG
Nonproprietary name
Rhus Aconitum
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Substance
ACONITUM NAPELLUS; ATROPA BELLADONNA; GELSEMIUM SEMPERVIRENS ROOT; MANDRAGORA OFFICINARUM ROOT; PENOXSULAM; PSEUDOGNAPHALIUM LUTEOALBUM LEAF; TOXICODENDRON PUBESCENS LEAF
Active strength
6; 6; 4; 6; 10; 4; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Rhus Aconitum
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACONITUM NAPELLUS6 [hp_X]/mL
ATROPA BELLADONNA6 [hp_X]/mL
GELSEMIUM SEMPERVIRENS ROOT4 [hp_X]/mL
MANDRAGORA OFFICINARUM ROOT6 [hp_X]/mL
PENOXSULAM10 [hp_X]/mL
PSEUDOGNAPHALIUM LUTEOALBUM LEAF4 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF6 [hp_X]/mL

Harmonized Identifiers#

Field, Values table
FieldValues
UniiU0NQ8555JD, WQZ3G9PF0H, 639KR60Q1Q, I2XCB174VB, 784ELC1SCZ, BGI20Z6M57, 6IO182RP7A

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8140-1Rhus Aconitum1 mL in 1 AMPULELIQUID15
48951-8140-1Rhus Aconitum10 in 1 BOXLIQUID105

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ACONITUM NAPELLUSACTIVE INGREDIENTU0NQ8555JDRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
ATROPA BELLADONNAACTIVE INGREDIENTWQZ3G9PF0HRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
GELSEMIUM SEMPERVIRENS ROOTACTIVE INGREDIENT639KR60Q1QRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
MANDRAGORA OFFICINARUM ROOTACTIVE INGREDIENTI2XCB174VBRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
PENOXSULAMACTIVE INGREDIENT784ELC1SCZRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
PSEUDOGNAPHALIUM LUTEOALBUM LEAFACTIVE INGREDIENTBGI20Z6M57RHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
TOXICODENDRON PUBESCENS LEAFACTIVE INGREDIENT6IO182RP7ARHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
ACONITUM NAPELLUSACTIVE MOIETYU0NQ8555JDRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
ATROPA BELLADONNAACTIVE MOIETYWQZ3G9PF0HRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
GELSEMIUM SEMPERVIRENS ROOTACTIVE MOIETY639KR60Q1QRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
MANDRAGORA OFFICINARUM ROOTACTIVE MOIETYI2XCB174VBRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
PENOXSULAMACTIVE MOIETY784ELC1SCZRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
PSEUDOGNAPHALIUM LUTEOALBUM LEAFACTIVE MOIETYBGI20Z6M57RHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
TOXICODENDRON PUBESCENS LEAFACTIVE MOIETY6IO182RP7ARHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RRHUS ACONITUM LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8140RHUS ACONITUM LIQUID [URIEL PHARMACY INC.]4Current NDC, Legacy NDC, 2 package rows20240120_a176c241-fc2d-4fea-82d9-81183971b4cf.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8140-14895181400110 AMPULE in 1 BOX (48951-8140-1) / 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent