Home NDC 51824-049 CareALL Non Aspirin
Product NDC 51824-049
11-digit product format 518240049
Labeler code 51824
Product ID 51824-049_44eb305c-ea53-afa4-e063-6394a90a9172
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form TABLET
Route ORAL
Labeler New World Imports, Inc
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-09-17
Marketing end 2026-07-01
Substance ACETAMINOPHEN
Active strength 500 mg/1
NDC exclude flag No
Current FDA listing Yes NDC auxiliary status# Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status.
Dataset, Scope, Product NDC table Dataset Scope Product NDC Package NDC Code Status Reporting period Source date excluded product product 51824-049 D Discontinued by firm 2026-07-31 excluded package package 51824-049 51824-049-24 D Discontinued by firm 2026-07-31
openFDA label cross-check# Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report.
Warnings cross-check# openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
warnings Warnings Liver warning: This product contains acetaminophen. The maximum daily dose of this product is 10 tablets (3,250 mg) in 24 hours for adults or 5 tablets (1,625 mg) in 24 hours for children. Severe liver damage may occur if ■ adult takes more than 4,000 mg of acetaminophen in 24 hours ■ child takes more than 5 doses in 24 hours, which is the maximum daily amount ■ taken with other drugs containing acetaminophen ■ adult has 3 or more alcoholic drinks every day while using this product Allergy alert: acetaminophen may cause severe skin reactions. Symptoms may include: ■ skin reddening ■ blisters ■ rash If a skin reaction occurs, stop use and seek medical help right away.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51824-049-01 CareALL Non AspirinExtra Strength 100 in 1 BOTTLE TABLET 100 6 51824-049-24 CareALL Non AspirinExtra Strength 24 in 1 CASE TABLET 24 6
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded Acetaminophen ACTIVE INGREDIENT 362O9ITL9D CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1 Acetaminophen ACTIVE MOIETY 362O9ITL9D CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1 Povidone INACTIVE INGREDIENT FZ989GH94E CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1 Propylene Glycol INACTIVE INGREDIENT 6DC9Q167V3 CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1 Sodium Starch Glycolate Type A Potato INACTIVE INGREDIENT 5856J3G2A2 CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1 STARCH, CORN INACTIVE INGREDIENT O8232NY3SJ CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1 Stearic Acid INACTIVE INGREDIENT 4ELV7Z65AP CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51824-049 CAREALL NON ASPIRIN EXTRA STRENGTH (ACETAMINOPHEN) TABLET [NEW WORLD IMPORTS, INC] 5 Current NDC, Legacy NDC, 2 package rows 20241009_5b5c2fd2-7ebf-4970-af68-3bef9ccddf91.zip
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 51824-049-01 51824004901 100 in 1 BOTTLE Historical 51824-049-24 51824004924 24 BOTTLE in 1 CASE (51824-049-24) / 100 TABLET in 1 BOTTLE (51824-049-01) 24 bottle 2015-09-17 2026-07-01 No No Current