Home NDC 82706-022 AXIV DayTime - Liquid
Product NDC 82706-022
11-digit product format 827060022
Labeler code 82706
Product ID 82706-022_3f018b49-e425-34a4-e063-6294a90adfa0
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen, Dextromethorphan Hydrobromide
Dosage form LIQUID
Route ORAL
Labeler VIVUNT PHARMA LLC
Application M012
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-05-14
Substance ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE
Active strength 650; 20 mg/30mL; mg/30mL
Pharmacologic classes Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes 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 AXIV DayTime - Liquid
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 650 mg/30mL DEXTROMETHORPHAN HYDROBROMIDE 20 mg/30mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup 9D2RTI9KYH Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 2604561 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 82706-022-01 AXIV DayTime - Liquid 355 mL in 1 BOTTLE, PLASTIC LIQUID 355 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 82706-022 AXIV DAYTIME - LIQUID (ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE) LIQUID [VIVUNT PHARMA LLC] 4 Current NDC, 1 package rows 20241010_1872e1ff-2e08-c404-e063-6294a90afa14.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 73 of 178 · 3,551 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 82706-022-01 82706002201 355 mL in 1 BOTTLE, PLASTIC (82706-022-01) 355 ml 2024-05-14 No No Current