Rosmarinus e fol. 1% Special Order

Product NDC
48951-8155
Requested package NDC
48951-8155-1
11-digit product format
489518155
Labeler code
48951
Product ID
48951-8155_6d07ab42-4d64-a092-e053-2991aa0a090c
Type
HUMAN OTC DRUG
Nonproprietary name
Rosmarinus e fol. 1% 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
ROSMARINUS OFFICINALIS FLOWERING TOP
Active strength
2 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-815548951-8155-1DDiscontinued by firm2026-07-31

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ROSMARINUS OFFICINALIS FLOWERING TOPACTIVE INGREDIENT8JM482TI79ROSMARINUS E FOL. 1% SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
ROSMARINUS OFFICINALIS FLOWERING TOPACTIVE MOIETY8JM482TI79ROSMARINUS E FOL. 1% SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
SODIUM CHLORIDEINACTIVE INGREDIENT451W47IQ8XROSMARINUS E FOL. 1% SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1
WATERINACTIVE INGREDIENT059QF0KO0RROSMARINUS E FOL. 1% SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-8155-14895181550110 AMPULE in 1 BOX (48951-8155-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent