Basic Care Dual Action

Product NDC
72288-530
11-digit product format
722880530
Labeler code
72288
Product ID
72288-530_2c38314b-424d-4002-9ff3-90cf42e6faca
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen, Ibuprofen
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Amazon.com Services LLC
Application
ANDA214836
Marketing category
ANDA
Marketing start
2023-08-14
Substance
ACETAMINOPHEN; IBUPROFEN
Active strength
250; 125 mg/1; mg/1
Pharmacologic classes
Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
362O9ITL9DACETAMINOPHEN103-90-2ACETAMINOPHEN
WK2XYI10QMIBUPROFEN15687-27-1IBUPROFEN

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
72288-530-01722880530011 BOTTLE in 1 CARTON (72288-530-01) / 216 TABLET, FILM COATED in 1 BOTTLE1 bottle2023-08-14NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Amazon Dual Action Drug FactsAmazon.com Services LLC2024-02-20HUMAN OTC DRUG LABEL2