Sinus Relief

Product NDC
0363-0524
11-digit product format
003630524
Labeler code
0363
Product ID
0363-0524_b4af45c3-34ef-45c9-8696-61f238c9a32c
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen, Dextromethorphan HBR, Guaifenesin, Phenylephrine HCl
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Walgreens
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2017-04-30
Marketing end
2024-05-31
Substance
ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
Active strength
325 mg/1; mg/1; mg/1; mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-0524-16EA - Each0363-052481c01ce4-394c-4844-9cc9-94bef039b92a12022-06-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-0524-16003630524162 BLISTER PACK in 1 CARTON (0363-0524-16) > 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK2 blister pack2017-04-300000-00-00NoNoCurrent