Home NDC 55910-282 Pain Relief
Product NDC 55910-282
11-digit product format 559100282
Labeler code 55910
Product ID 55910-282_f66383d7-f9b3-42cd-805d-b9c47d19a4e6
Type HUMAN OTC DRUG
Nonproprietary name Acetaminophen
Dosage form SUSPENSION
Route ORAL
Labeler Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application M013
Marketing category OTC MONOGRAPH DRUG
Marketing start 2015-04-30
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 Pain Relief
Brand name suffix Childrens
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 55910-282-08 Pain ReliefChildrens 1 in 1 BOX SUSPENSION 1 8 55910-282-08 Pain ReliefChildrens 237 mL in 1 BOTTLE, PLASTIC SUSPENSION 237 8
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded ACETAMINOPHEN ACTIVE INGREDIENT 362O9ITL9D PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 ACETAMINOPHEN ACTIVE MOIETY 362O9ITL9D PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 ACESULFAME POTASSIUM INACTIVE INGREDIENT 23OV73Q5G9 PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 ANHYDROUS CITRIC ACID INACTIVE INGREDIENT XF417D3PSL PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 BUTYLPARABEN INACTIVE INGREDIENT 3QPI1U3FV8 PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM INACTIVE INGREDIENT K679OBS311 PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 CELLULOSE, MICROCRYSTALLINE INACTIVE INGREDIENT OP1R32D61U PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 FD&C RED NO. 40 INACTIVE INGREDIENT WZB9127XOA PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 GLYCERIN INACTIVE INGREDIENT PDC6A3C0OX PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 HIGH FRUCTOSE CORN SYRUP INACTIVE INGREDIENT XY6UN3QB6S PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 PROPYLENE GLYCOL INACTIVE INGREDIENT 6DC9Q167V3 PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 SODIUM BENZOATE INACTIVE INGREDIENT OJ245FE5EU PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 SORBITOL INACTIVE INGREDIENT 506T60A25R PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 WATER INACTIVE INGREDIENT 059QF0KO0R PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1 XANTHAN GUM INACTIVE INGREDIENT TTV12P4NEE PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 1
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 55910-282 PAIN RELIEF CHILDRENS (ACETAMINOPHEN) SUSPENSION [DOLGENCORP, INC. (DOLLAR GENERAL & REXALL)] 8 Current NDC, Legacy NDC, 2 package rows 20231207_41633554-474e-4d3c-9187-d90487d2ae8c.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 13 of 79 · 1,579 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Marketing end Sample Exclude flag Status 55910-282-08 55910028208 1 BOTTLE, PLASTIC in 1 BOX (55910-282-08) / 237 mL in 1 BOTTLE, PLASTIC 2015-04-30 0000-00-00 No No Current