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Product NDC
41520-806
11-digit product format
415200806
Labeler code
41520
Product ID
41520-806_b152519f-0778-484d-b34a-ec5f52f5c939
Type
HUMAN OTC DRUG
Nonproprietary name
acetaminophen, guaifenesin, phenylephrine hydrochloride, diphenhydramine hydrochloride
Dosage form
KIT
Labeler
American Sales Company
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2019-10-08
Marketing end
0000-00-00
Active strength
0
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
41520-806-802025-02-05C16284748780-12cef2736-75d7-d83d-e063-dadaa90ab31fb152519f-0778-484d-b34a-ec5f52f5c939
41520-806-802025-01-30C16284748780-12cef2736-75d7-d83d-e063-dadaa90ab31fb152519f-0778-484d-b34a-ec5f52f5c939

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41520-806-80415200806801 KIT in 1 KIT (41520-806-80) * 2 TABLET, FILM COATED in 1 BLISTER PACK * 2 TABLET, FILM COATED in 1 BLISTER PACK1 kit2019-10-080000-00-00NoNoCurrent