Home NDC 69842-071-04 Maximum Strength Nighttime Cold/Flu Relief
Product NDC 69842-071
Requested package NDC 69842-071-04
11-digit product format 698420071
Labeler code 69842
Product ID 69842-071_cf195dcc-7557-4b4e-bd8d-140ad35ffbe0
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Dextromethorphan HBr, Doxylamine succinate, Phenylephrine HCI
Dosage form CAPSULE, LIQUID FILLED
Route ORAL
Labeler CVS PHARMACY, INC.
Application part341
Marketing category OTC MONOGRAPH FINAL
Marketing start 2016-12-14
Marketing end 0000-00-00
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
Active strength 325 mg/1; mg/1; mg/1; mg/1
NDC exclude flag No
Listing certified through 2020-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 9 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Code, Status table Captured / source date Code Status Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 I Inactivated by FDA d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 I Inactivated by FDA f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 I Inactivated by FDA 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 I Inactivated by FDA a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 I Inactivated by FDA cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 I Inactivated by FDA cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 U Excluded because listing certification expired 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 U Excluded because listing certification expired ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 U Excluded because listing certification expired 0efc9e666f02…f202fb6c5f17…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Product Concepts# FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69842-071-04 Maximum Strength Nighttime Cold/Flu Relief 2 in 1 CARTON CAPSULE, LIQUID FILLED 2 1 69842-071-04 Maximum Strength Nighttime Cold/Flu Relief 12 in 1 BLISTER PACK CAPSULE, LIQUID FILLED 12 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-071 MAXIMUM STRENGTH NIGHTTIME COLD/FLU RELIEF (ACETAMINOPHEN, DEXTROMETHORPHAN HBR, DOXYLAMINE SUCCINATE, PHENYLEPHRINE HCI) CAPSULE, LIQUID FILLED [CVS PHARMACY, INC.] 1 Legacy NDC, 2 package rows 20161214_5612afac-0b19-4c76-b705-b59c5416fb35.zip
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 69842-071-04 69842007104 2 BLISTER PACK in 1 CARTON (69842-071-04) > 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK 2 blister pack 2016-12-14 0000-00-00 No No Current