Cinis Equiseti 6

Product NDC
48951-3235
Requested package NDC
48951-3235-3
11-digit product format
489513235
Labeler code
48951
Product ID
48951-3235_b6864e87-38cd-d5d6-e053-2a95a90a6881
Type
HUMAN OTC DRUG
Nonproprietary name
Cinis Equiseti 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
EQUISETUM ARVENSE TOP
Active strength
6 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

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

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded packagepackage48951-323548951-3235-3IInactivated by FDA2026-08-17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3235-3Cinis Equiseti 660 mL in 1 BOTTLE, DROPPERLIQUID607

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3235CINIS EQUISETI 6 LIQUID [URIEL PHARMACY INC.]7Legacy NDC, 1 package rows20241116_b633713a-35fd-11e4-e053-2a95a90a3e1d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3235-34895132350360 mL in 1 BOTTLE, DROPPER (48951-3235-3) 60 ml2009-09-010000-00-00NoNoCurrent