Home NDC 69842-820 Multi Symptom Cold and Multi Symptom Nighttime Cold
Product NDC 69842-820
11-digit product format 698420820
Labeler code 69842
Product ID 69842-820_6c0a3bbd-d6cc-4c17-a731-7d6f801daa77
Type HUMAN OTC DRUG
Nonproprietary name Dextromethorphan HBr, Guaifenesin, Phenylephrine HCI, Acetaminophen, Diphenhydramine HCI, Phenylephrine HCI
Dosage form KIT
Labeler CVS Pharmacy
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-02-28
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes 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 · 2 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-03-10 12:48 UTC · source 2025-03-10 excluded product product 69842-820 D Discontinued by firm excluded / ndc_excluded.zip cdf11ea48f46…ba0047e9e063…2025-03-10 12:48 UTC · source 2025-03-10 excluded package package 69842-820 69842-820-08 D Discontinued by firm excluded / ndc_excluded.zip cdf11ea48f46…ba0047e9e063…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Multi Symptom Cold and Multi Symptom Nighttime Cold
Brand name suffix Childrens
Listing expiration 2027-12-31 Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 3 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1043543 Internal RxNorm lookup 1375932 Internal RxNorm lookup 2637728 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69842-606-04 Multi Symptom Cold and Multi Symptom Nighttime ColdChildrens 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 mL 5 mg in 10mL 6 69842-607-04 Multi Symptom Cold and Multi Symptom Nighttime ColdChildrens 118 mL in 1 BOTTLE, PLASTIC LIQUID 118 mL 5 mg in 5mL 6 69842-820-08 Multi Symptom Cold and Multi Symptom Nighttime ColdChildrens 1 in 1 KIT KIT 1 6
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69842-820 MULTI SYMPTOM COLD AND MULTI SYMPTOM NIGHTTIME COLD CHILDRENS (DEXTROMETHORPHAN HBR, GUAIFENESIN, PHENYLEPHRINE HCI, ACETAMINOPHEN, DIPHENHYDRAMINE HCI, PHENYLEPHRINE HCI) KIT [CVS PHARMACY] 5 Current NDC, Legacy NDC, 3 package rows 20250316_ebf2dbb4-96fa-4bf6-9afd-8aa8b5369f2e.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 74 of 180 · 3,583 matching rows.
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 69842-606-04 69842060604 118 mL in 1 BOTTLE, PLASTIC 118 ml Historical 69842-607-04 69842060704 118 mL in 1 BOTTLE, PLASTIC 118 ml Historical 69842-820-08 69842082008 1 KIT in 1 KIT (69842-820-08) * 118 mL in 1 BOTTLE, PLASTIC (69842-607-04) * 118 mL in 1 BOTTLE, PLASTIC (69842-606-04) 1 kit 2017-02-28 2025-02-28 No No Current