Dermveda ULTRA BITE ITCH RELIEF

Product NDC
83819-106
11-digit product format
838190106
Labeler code
83819
Product ID
83819-106_f0ecbd75-2453-42c5-9ca7-03a3a6fabe65
Type
HUMAN OTC DRUG
Nonproprietary name
Mentha Piperita, Curcuma Longa
Dosage form
CREAM
Route
TOPICAL
Labeler
Celcius Corp.
Marketing category
UNAPPROVED HOMEOPATHIC
Marketing start
2024-09-18
Substance
MENTHA X PIPERITA WHOLE; TURMERIC
Active strength
10; 10 [hp_X]/60mL; [hp_C]/60mL
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Dermveda ULTRA BITE ITCH RELIEF
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MENTHA X PIPERITA WHOLE10 [hp_X]/60mL
TURMERIC10 [hp_C]/60mL

Harmonized Identifiers#

Field, Values table
FieldValues
Unii79M2M2UDA9, 856YO1Z64F

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83819-106-02Dermveda ULTRA BITE ITCH RELIEF60 mL in 1 JARCREAM602

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83819-106DERMVEDA ULTRA BITE ITCH RELIEF (MENTHA PIPERITA, CURCUMA LONGA) CREAM [CELCIUS CORP.]1Current NDC, 1 package rows20241004_232c344e-184d-4c95-bc2c-97c4c9cab091.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
83819-106-028381901060260 mL in 1 JAR (83819-106-02) 60 ml2024-09-18NoNoHistorical