Nux vomica e sem. 6 Special Order

Product NDC
48951-7134
11-digit product format
489517134
Labeler code
48951
Product ID
48951-7134_6ad81326-94ce-9ac8-e053-2991aa0a9e7f
Type
HUMAN OTC DRUG
Nonproprietary name
Nux vomica e sem. 6 Special Order
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
STRYCHNOS NUX-VOMICA SEED
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
48951-7134-1Nux vomica e sem. 6 Special Order10 in 1 BOXLIQUID103
48951-7134-1Nux vomica e sem. 6 Special Order1 mL in 1 AMPULELIQUID13

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
STRYCHNOS NUX-VOMICA SEEDACTIVE INGREDIENT269XH13919NUX VOMICA E SEM. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
STRYCHNOS NUX-VOMICA SEEDACTIVE MOIETY269XH13919NUX VOMICA E SEM. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XNUX VOMICA E SEM. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RNUX VOMICA E SEM. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-7134NUX VOMICA E SEM. 6 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]3Legacy NDC, 2 package rows20180427_f9aa8856-3504-4b03-b77c-3e321517e07b.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-7134-14895171340110 AMPULE in 1 BOX (48951-7134-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent