Childrens Pain and Fever

Product NDC
0363-5101
11-digit product format
003635101
Labeler code
0363
Product ID
0363-5101_446a2332-4899-48c7-e063-6294a90a291f
Type
HUMAN OTC DRUG
Nonproprietary name
Acetaminophen
Dosage form
POWDER
Route
ORAL
Labeler
WALGREENS CO.
Application
M013
Marketing category
OTC MONOGRAPH DRUG
Marketing start
2020-01-29
Substance
ACETAMINOPHEN
Active strength
160 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Childrens Pain and Fever
Brand name suffix
Dissolve Packs
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
ACETAMINOPHEN160 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii362O9ITL9D
Rxcui2178755

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-5101-18Childrens Pain and FeverDissolve Packs1 in 1 PACKETPOWDER17
0363-5101-18Childrens Pain and FeverDissolve Packs18 in 1 CARTONPOWDER187

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0363-5101CHILDRENS PAIN AND FEVER DISSOLVE PACKS (ACETAMINOPHEN) POWDER [WALGREENS CO.]6Current NDC, Legacy NDC, 2 package rows20241110_ea0f265f-7d64-4731-beda-0bb841dd1ad7.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
2178755acetaminophen 160 MG Oral PowderPSNea0f265f-7d64-4731-beda-0bb841dd1ad77
2178755acetaminophen 160 MG Oral PowderSCDea0f265f-7d64-4731-beda-0bb841dd1ad77
2178755APAP 160 MG Oral PowderSYea0f265f-7d64-4731-beda-0bb841dd1ad77

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-5101-180036351011818 PACKET in 1 CARTON (0363-5101-18) / 1 POWDER in 1 PACKET18 packet2020-01-290000-00-00NoNoCurrent