Calendula 10%

Product NDC
48951-4165
Requested package NDC
48951-4165-5
11-digit product format
489514165
Labeler code
48951
Product ID
48951-4165_c19b1db8-df52-e8fc-e053-2a95a90aee03
Type
HUMAN OTC DRUG
Nonproprietary name
Calendula 10%
Dosage form
GEL
Route
TOPICAL
Labeler
Uriel Pharmacy Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
CALENDULA OFFICINALIS FLOWERING TOP
Active strength
1 [hp_X]/g
NDC exclude flag
No
Listing certified through
2022-12-31
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 packagepackage48951-416548951-4165-5IInactivated by FDA2026-08-17

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-4165-5Calendula 10%60 g in 1 TUBEGEL602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-4165CALENDULA 10% GEL [URIEL PHARMACY INC.]2Legacy NDC, 1 package rows20240319_c19b1db8-df51-e8fc-e053-2a95a90aee03.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-4165-54895141650560 g in 1 TUBE (48951-4165-5) 60 g2009-09-010000-00-00NoNoCurrent