AC Control Serum

Product NDC
70380-070
11-digit product format
703800070
Labeler code
70380
Product ID
70380-070_7898579a-57a4-45d2-9a52-127cd6a4f487
Type
HUMAN OTC DRUG
Nonproprietary name
Allantoin
Dosage form
CREAM
Route
TOPICAL
Labeler
MIGUHARA
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2016-01-02
Marketing end
0000-00-00
Substance
ALLANTOIN
Active strength
0 g/50mL
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
70380-070-012020-01-31C16284748780-19d75b9d0-4ad7-f424-e053-dadaa90a57ce7bd6ae6a-5414-4595-a986-7dfccfd01572

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
70380-070-01AC Control Serum50 mL in 1 CARTONCREAM501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70380-070AC CONTROL SERUM (ALLANTOIN) CREAM [MIGUHARA]1Legacy NDC, 1 package rows20160218_7bd6ae6a-5414-4595-a986-7dfccfd01572.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsStatus
70380-070-017038000700150 mL in 1 CARTON50 mlHistorical