Home NDC 71205-314 MEDI-FIRST Non-Aspirin Extra Strength
Product NDC 71205-314
11-digit product format 712050314
Labeler code 71205
Product ID 71205-314_9608b190-4f25-48f2-a49c-11c360656608
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET, FILM COATED
Route ORAL
Labeler Proficient Rx LP
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2008-12-30
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Listing certified through 2027-12-31
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 MEDI-FIRST Non-Aspirin Extra Strength
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 500 mg/1
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 362O9ITL9D Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 198440 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71205-314-04 MEDI-FIRST Non-Aspirin Extra Strength 4 in 1 PACKET TABLET, FILM COATED 4 4 71205-314-08 MEDI-FIRST Non-Aspirin Extra Strength 8 in 1 PACKET TABLET, FILM COATED 8 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71205-314 MEDI-FIRST NON-ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET, FILM COATED [PROFICIENT RX LP] 4 Current NDC, Legacy NDC, 2 package rows 20240201_9071b047-5463-4f65-b775-bfb0ce066527.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 2 of 83 · 1,657 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 71205-314-04 71205031404 4 TABLET, FILM COATED in 1 PACKET (71205-314-04) 2019-09-01 0000-00-00 No No Current 71205-314-08 71205031408 8 TABLET, FILM COATED in 1 PACKET (71205-314-08) 2020-02-05 0000-00-00 No No Current