Skin-ion

Product NDC
49742-1001
11-digit product format
497421001
Labeler code
49742
Product ID
49742-1001_8089b888-7b55-44ea-a12a-6ab827edf4e8
Type
HUMAN OTC DRUG
Nonproprietary name
ARBUTIN, ADENOSINE, GLYCERIN
Dosage form
SPRAY
Route
TOPICAL
Labeler
WAKO Korea Corp
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2010-01-01
Marketing end
0000-00-00
Substance
ARBUTIN; ADENOSINE; GLYCERIN
Active strength
1 mL/40mL; mL/40mL; mL/40mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d676a241-be05-4740-b3ee-1a5f2ed422d2Product name420180615
dd8bd48f-20d6-43c7-b471-3ae872868afaProduct name320180125
d41954ff-bc63-4b2c-aba0-9146707659d7Product name220151117

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49742-1001-12019-10-21C16284748780-1956f9ecf-dd85-621f-e053-dbdaa90a74ad6fc39322-244c-4f35-a983-c994ac17632a

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49742-1001-1Skin-ion40 mL in 1 CARTONSPRAY401

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49742-1001SKIN-ION (ARBUTIN, ADENOSINE, GLYCERIN) SPRAY [WAKO KOREA CORP]1Legacy NDC, 1 package rows20100101_6fc39322-244c-4f35-a983-c994ac17632a.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
49742-1001-14974210010140 mL in 1 CARTON40 mlHistorical