Home NDC 69729-118 Neo-Lubrina
Product NDC 69729-118
11-digit product format 697290118
Labeler code 69729
Product ID 69729-118_5c3f9d3e-5df2-1696-e063-6394a90a5154
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form SUSPENSION
Route ORAL
Labeler OPMX Chula Vista
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-06-02
Substance ACETAMINOPHEN
Active strength 160 mg/5mL
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 Neo-Lubrina
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ACETAMINOPHEN 160 mg/5mL
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69729-118-04 Neo-Lubrina 118 mL in 1 BOTTLE SUSPENSION 118 4 69729-118-04 Neo-Lubrina 1 in 1 CARTON SUSPENSION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69729-118 NEO-LUBRINA (ACETAMINOPHEN) SUSPENSION [OPMX CHULA VISTA] 4 Current NDC, 2 package rows 20241116_fd3ca168-23b9-3eb8-e053-6394a90ac89b.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 1 of 83 · 1,657 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 69729-118-04 69729011804 1 BOTTLE in 1 CARTON (69729-118-04) / 118 mL in 1 BOTTLE 1 bottle 2023-06-02 No No Current