THE SKINHOUSE WRINKLE SUPREME TONER

Product NDC
73590-0008
11-digit product format
735900008
Labeler code
73590
Product ID
73590-0008_9d530096-d5ba-5c06-e053-2995a90a60d9
Type
HUMAN OTC DRUG
Nonproprietary name
Panax Ginseng Root Extract
Dosage form
LIQUID
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
73590-0008-12025-01-30C16284748780-12cef2736-921d-d83d-e063-dadaa90ab31fDrug Facts

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73590-0008-1THE SKINHOUSE WRINKLE SUPREME TONER130 mL in 1 BOTTLELIQUID1301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73590-0008THE SKINHOUSE WRINKLE SUPREME TONER (PANAX GINSENG ROOT EXTRACT) LIQUID [NOKSIBCHO COSMETIC CO., LTD.]1Legacy NDC, 1 package rows20200130_9d52ec6d-72af-112f-e053-2995a90a1ac3.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
73590-0008-173590000801130 mL in 1 BOTTLE (73590-0008-1) 130 ml2020-01-220000-00-00NoNoCurrent