Luxury Cell Performance Emulsion

Product NDC
60949-130
11-digit product format
609490130
Labeler code
60949
Product ID
60949-130_74318e49-75c9-4d0a-a2d3-bce48ca030fb
Type
HUMAN OTC DRUG
Nonproprietary name
ALLANTOIN
Dosage form
CREAM
Route
TOPICAL
Labeler
Pharmicell Co., Ltd.
Application
part347
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2014-08-01
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
1 mg/130mL
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
60949-130-012019-11-27C16284748780-19855e2a2-46fb-60a7-e053-dbdaa90a05bd7eab83fb-72a5-4e74-8015-40df3b6465a5

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
60949-130-01Luxury Cell Performance Emulsion130 mL in 1 CARTONCREAM1301

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
60949-130LUXURY CELL PERFORMANCE EMULSION (ALLANTOIN) CREAM [PHARMICELL CO., LTD.]1Legacy NDC, 1 package rows20140922_7eab83fb-72a5-4e74-8015-40df3b6465a5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
60949-130-0160949013001130 mL in 1 CARTON130 mlHistorical