Home NDC 59779-590-10 infants pain and fever
Product NDC 59779-590
Requested package NDC 59779-590-10
11-digit product format 597790590
Labeler code 59779
Product ID 59779-590_a34699ac-20ae-4ca6-a2c0-20003a0c42e7
Type HUMAN OTC DRUG
Nonproprietary name acetaminophen
Dosage form SUSPENSION
Route ORAL
Labeler CVS Pharmacy
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 1993-04-30
Substance ACETAMINOPHEN
Active strength 160 mg/5mL
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 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
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 infants pain and fever
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.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 59779-590-10 infants pain and fever 30 mL in 1 BOTTLE SUSPENSION 30 6 59779-590-10 infants pain and fever 1 in 1 CARTON SUSPENSION 1 6 59779-590-16 infants pain and fever 1 in 1 CARTON SUSPENSION 1 6 59779-590-16 infants pain and fever 59 mL in 1 BOTTLE SUSPENSION 59 6 59779-590-26 infants pain and fever 1 in 1 CARTON SUSPENSION 1 6 59779-590-26 infants pain and fever 118 mL in 1 BOTTLE SUSPENSION 118 6
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 59779-590 INFANTS PAIN AND FEVER (ACETAMINOPHEN) SUSPENSION [CVS PHARMACY] 6 Current NDC, Legacy NDC, 6 package rows 20240830_53b06c48-598e-41ad-ac7a-5508c195535c.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 Marketing end Sample Exclude flag Status 59779-590-10 59779059010 1 BOTTLE in 1 CARTON (59779-590-10) > 30 mL in 1 BOTTLE 1 bottle 2011-12-07 0000-00-00 No No Current