Zernel Scalp Rejuver Essence

Product NDC
80152-302
11-digit product format
801520302
Labeler code
80152
Product ID
80152-302_be2d5be9-77e8-80e2-e053-2995a90a6c87
Type
HUMAN OTC DRUG
Nonproprietary name
Salicylic Acid
Dosage form
LIQUID
Route
TOPICAL
Labeler
ZINOZEN CO., LTD.
Application
part358H
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2021-05-07
Marketing end
0000-00-00
Substance
SALICYLIC ACID
Active strength
0 mg/100mL
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627
0ca1d589-929b-4b33-bc5b-1d84abdafa6aProduct name120150324
fc363c46-397b-4476-ac0f-70e43e8e4592Product name120150324
1681bc73-b05f-12c3-1075-382ae39f449cProduct name120140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
80152-302-012022-07-29C16284748780-1e4f33bdf-aeab-d8a0-e053-dadaa90a6e4e80152-303 SCALP REJUVER ESSENCE

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
80152-302-01Zernel Scalp Rejuver Essence200 mL in 1 BOTTLELIQUID2001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
80152-302ZERNEL SCALP REJUVER ESSENCE (SALICYLIC ACID) LIQUID [ZINOZEN CO., LTD.]1Legacy NDC, 1 package rows20210508_be2d5be9-77e7-80e2-e053-2995a90a6c87.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
80152-302-0180152030201200 mL in 1 BOTTLE (80152-302-01) 200 ml2021-05-070000-00-00NoNoCurrent