Equisetum limosum Rubellite 30

Product NDC
48951-4038
11-digit product format
489514038
Labeler code
48951
Product ID
48951-4038_6c6c3cea-8514-6b60-e053-2a91aa0a60e7
Type
HUMAN OTC DRUG
Nonproprietary name
Equisetum limosum Rubellite 30
Dosage form
LIQUID
Route
ORAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
EQUISETUM ARVENSE TOP; SILICON DIOXIDE
Active strength
30 [hp_X]/mL; [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
48951-4038-1Equisetum limosum Rubellite 301 mL in 1 AMPULELIQUID14
48951-4038-1Equisetum limosum Rubellite 3010 in 1 BOXLIQUID104

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4038EQUISETUM LIMOSUM RUBELLITE 30 LIQUID [URIEL PHARMACY INC.]4Legacy NDC, 2 package rows20240118_f4989f37-1743-487c-8b85-bc7380569508.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4038-14895140380110 AMPULE in 1 BOX (48951-4038-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent