THE SKINHOUSE WRINKLE SUPREMEEMULSION

Product NDC
73590-0006
11-digit product format
735900006
Labeler code
73590
Product ID
73590-0006_9d526616-5b33-9195-e053-2995a90a59bb
Type
HUMAN OTC DRUG
Nonproprietary name
Panax Ginseng Root Extract
Dosage form
EMULSION
Route
TOPICAL
Labeler
NOKSIBCHO cosmetic Co., Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2020-01-22
Marketing end
0000-00-00
Substance
ASIAN GINSENG
Active strength
1 g/100mL
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
73590-0006-12025-01-30C16284748780-12cef2736-b030-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73590-0006-1THE SKINHOUSE WRINKLE SUPREMEEMULSION130 mL in 1 BOTTLEEMULSION1301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73590-0006THE SKINHOUSE WRINKLE SUPREMEEMULSION (PANAX GINSENG ROOT EXTRACT) EMULSION [NOKSIBCHO COSMETIC CO., LTD.]1Legacy NDC, 1 package rows20200130_9d527876-8ec2-5285-e053-2a95a90a1ba2.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73590-0006-173590000601130 mL in 1 BOTTLE (73590-0006-1) 130 ml2020-01-220000-00-00NoNoCurrent