Mucinex Fast-Max Day Time Severe Cold and Mucinex Fast-Max Night Time Cold and Flu

Product NDC
63824-557
11-digit product format
638240557
Labeler code
63824
Product ID
63824-557_a2cba0cd-fc98-49e6-a0c4-2b8a20fbcae9
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen, Dextromethorphan Hydrobromide, Diphenhydramine Hydrochloride, Guaifenesin, and Phenylephrine Hydrochloride
Dosage form
KIT
Labeler
Reckitt Benckiser LLC
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2015-08-25
Marketing end
0000-00-00
Active strength
0
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
63824-557-302023-09-07C16284748780-19d75b9d0-ac51-f424-e053-dadaa90a57cefa232c72-41ec-40b9-973d-5ba1b06b0614
63824-557-302020-01-31C16284748780-19d75b9d0-ac51-f424-e053-dadaa90a57cefa232c72-41ec-40b9-973d-5ba1b06b0614

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
63824-557-30EA - Each63824-557da184aa2-67ae-4ce8-ba72-a77fb6b581ac12017-09-11