FDA.reportPublic FDA data

GD11 Rx SCM C5

Product NDC
62171-100
11-digit product format
621710100
Labeler code
62171
Product ID
62171-100_bbc9fd79-64bd-4764-b770-eb6451853a2f
Type
HUMAN OTC DRUG
Nonproprietary name
MANNITOL
Dosage form
LIQUID
Route
TOPICAL
Labeler
Coson Co., Ltd.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2017-07-01
Marketing end
0000-00-00
Substance
MANNITOL
Active strength
0 g/2mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
d1c9d1af-bddd-448d-86f7-69052b7d5b47Product name120220627

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
62171-100-022025-11-09C16284748780-19d75b9d0-6100-f424-e053-dadaa90a57ce64654bc7-b829-430b-a382-eb776f5f0edb
62171-100-022020-01-31C16284748780-19d75b9d0-6100-f424-e053-dadaa90a57ce64654bc7-b829-430b-a382-eb776f5f0edb

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62171-100GD11 RX SCM C5 (MANNITOL) LIQUID [COSON CO., LTD.]1Legacy NDC20170824_64654bc7-b829-430b-a382-eb776f5f0edb.zip