Home NDC 69729-825-04 Mejoralito Children
Product NDC 69729-825
Requested package NDC 69729-825-04
11-digit product format 697290825
Labeler code 69729
Product ID 69729-825_5464188d-0138-033e-e063-6294a90ace66
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form SYRUP
Route ORAL
Labeler OPMX LLC
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-16
Substance ACETAMINOPHEN
Active strength 160 mg/5mL
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Mejoralito Children
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 160 mg/5mL
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 307668 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 1 of 85 · 1,687 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Status 69729-825-04 69729082504 1 BOTTLE in 1 CARTON (69729-825-04) / 118 mL in 1 BOTTLE 1 bottle 2026-06-16 0 Current