Threefold Balance

Product NDC
48951-9364
11-digit product format
489519364
Labeler code
48951
Product ID
48951-9364_de5bb0ae-ea91-d8df-e053-2a95a90ae964
Type
HUMAN OTC DRUG
Nonproprietary name
Threefold Balance
Dosage form
TABLET
Route
ORAL
Labeler
Uriel Pharmacy, Inc.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2009-09-01
Marketing end
0000-00-00
Substance
FRANKINCENSE; GOLD; MYRRH
Active strength
2 [hp_X]/1; [hp_X]/1; [hp_X]/1
Pharmacologic classes
Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
48951-9364-42026-01-29C16284748780-149896155-ac8f-586f-e063-e6dba90add90Threefold Balance

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-9364-4Threefold Balance230 in 1 BOTTLE, GLASSTABLET2302

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-9364THREEFOLD BALANCE TABLET [URIEL PHARMACY, INC.]2Legacy NDC, 1 package rows20240926_de5bb0ae-ea90-d8df-e053-2a95a90ae964.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
48951-9364-448951936404230 TABLET in 1 BOTTLE, GLASS (48951-9364-4) 230 tablet2009-09-010000-00-00NoNoCurrent