Chamomilla e rad. 3 Special Order

Product NDC
48951-3218
11-digit product format
489513218
Labeler code
48951
Product ID
48951-3218_6c57b631-c160-c139-e053-2991aa0a819e
Type
HUMAN OTC DRUG
Nonproprietary name
Chamomilla e rad. 3 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
MATRICARIA RECUTITA
Active strength
3 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2020-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
DatasetScopeProduct NDCPackage NDCCodeStatusReporting periodSource date
excluded productproduct48951-3218IInactivated by FDA2026-09-14
excluded packagepackage48951-321848951-3218-1IInactivated by FDA2026-09-14

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-3218-1Chamomilla e rad. 3 Special Order10 in 1 BOXLIQUID101
48951-3218-1Chamomilla e rad. 3 Special Order1 mL in 1 AMPULELIQUID11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-3218CHAMOMILLA E RAD. 3 SPECIAL ORDER LIQUID [URIEL PHARMACY INC.]1Legacy NDC, 2 package rows20180516_6c57b631-c15f-c139-e053-2991aa0a819e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-3218-14895132180110 AMPULE in 1 BOX (48951-3218-1) > 1 mL in 1 AMPULE10 ampule2009-09-010000-00-00NoNoCurrent