AAPE Skin Ampoule

Product NDC
62041-250
11-digit product format
620410250
Labeler code
62041
Product ID
62041-250_b5a74e09-959a-4bc2-a0f4-e0c9194a3231
Type
HUMAN OTC DRUG
Nonproprietary name
Niacinamide
Dosage form
LIQUID
Route
TOPICAL
Labeler
PROSTEMICS Co., Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2019-08-01
Marketing end
0000-00-00
Substance
NIACINAMIDE
Active strength
0 g/6mL
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62041-250-012024-01-30C16284748780-11030e365-5dd5-111a-e063-dadaa90a10e2a0cfe424-aeb1-48ba-9572-4e9885c842da

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62041-250-01AAPE Skin Ampoule6 mL in 1 CONTAINERLIQUID61

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62041-250AAPE SKIN AMPOULE (NIACINAMIDE) LIQUID [PROSTEMICS CO., LTD.]1Legacy NDC, 1 package rows20190826_a0cfe424-aeb1-48ba-9572-4e9885c842da.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
62041-250-01620410250016 mL in 1 CONTAINER (62041-250-01) 6 ml2019-08-010000-00-00NoNoCurrent