Theraworx Relief Joint Discomfort and Inflamation

Product NDC
71064-0013
11-digit product format
710640013
Labeler code
71064
Product ID
71064-0013_c0eb8a31-ad3b-1312-e053-2995a90af133
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
FRANKINCENSE
Dosage form
SOLUTION
Route
TOPICAL
Labeler
Relion Manufacturing
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2020-07-11
Marketing end
0000-00-00
Substance
FRANKINCENSE
Active strength
8 [hp_X]/mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71064-0013-32023-01-30C16284748780-1f386c64a-0a33-0266-e053-dadaa90a7c1aTheraworx Joint Discomfort and Inflamation Foam

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71064-0013-3Theraworx Relief Joint Discomfort and Inflamation101 mL in 1 BOTTLESOLUTION1011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71064-0013THERAWORX RELIEF JOINT DISCOMFORT AND INFLAMATION (FRANKINCENSE) SOLUTION [RELION MANUFACTURING]1Legacy NDC, 1 package rows20210427_c0eb654b-6fe7-46ab-e053-2a95a90aa9cd.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71064-0013-371064001303101 mL in 1 BOTTLE (71064-0013-3) 101 ml2020-07-110000-00-00NoNoCurrent