NDC 49738-519

Pain Relief Extra Strength

Acetaminophen

Pain Relief Extra Strength is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Kmart Corporation. The primary component is Acetaminophen.

Product ID49738-519_16ad31f0-56e0-42ec-9bc0-416410d11fe0
NDC49738-519
Product TypeHuman Otc Drug
Proprietary NamePain Relief Extra Strength
Generic NameAcetaminophen
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2004-05-10
Marketing End Date2021-02-28
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameKmart Corporation
Substance NameACETAMINOPHEN
Active Ingredient Strength500 mg/1
NDC Exclude FlagN

Packaging

NDC 49738-519-06

2 BOTTLE in 1 CARTON (49738-519-06) > 100 TABLET in 1 BOTTLE
Marketing Start Date2004-05-10
Marketing End Date2021-02-28
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49738-519-08 [49738051908]

Pain Relief Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10
Marketing End Date2021-02-28

NDC 49738-519-15 [49738051915]

Pain Relief Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10
Marketing End Date2021-02-28

NDC 49738-519-06 [49738051906]

Pain Relief Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10
Marketing End Date2021-02-28

NDC 49738-519-54 [49738051954]

Pain Relief Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10
Marketing End Date2021-02-28

NDC 49738-519-12 [49738051912]

Pain Relief Extra Strength TABLET
Marketing CategoryOTC MONOGRAPH NOT FINAL
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2004-05-10
Marketing End Date2021-02-28

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:1a1edec9-38c7-47d0-b4f5-1ace124e0339
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 198440
  • UPC Code
  • 0883967388127
  • NDC Crossover Matching brand name "Pain Relief Extra Strength" or generic name "Acetaminophen"

    NDCBrand NameGeneric Name
    69168-328Pain Relief Extra StrengthPain Relief Extra Strength
    69168-235Pain Relief Extra StrengthPain Relief Extra Strength
    69469-494Pain Relief Extra StrengthPain Relief Extra Strength
    69842-073Pain Relief Extra StrengthPain Relief Extra Strength
    11822-0812Pain Relief Extra StrengthPain Relief Extra Strength
    15127-857Pain Relief Extra StrengthPain Relief Extra Strength
    21130-919Pain Relief Extra StrengthPain Relief Extra Strength
    21130-975Pain Relief Extra StrengthPain Relief Extra Strength
    33992-0519Pain Relief Extra StrengthPain Relief Extra Strength
    36800-904Pain Relief Extra StrengthPain Relief Extra Strength
    36800-770Pain Relief Extra StrengthPain Relief Extra Strength
    36800-905Pain Relief Extra StrengthPain Relief Extra Strength
    37808-195Pain Relief Extra StrengthPain Relief Extra Strength
    37012-227Pain Relief Extra StrengthPain Relief Extra Strength
    37808-704Pain Relief Extra StrengthPain Relief Extra Strength
    37808-792Pain Relief Extra StrengthPain Relief Extra Strength
    41250-875Pain Relief Extra StrengthPain Relief Extra Strength
    42507-484pain relief extra strengthpain relief extra strength
    46122-370Pain Relief Extra StrengthPain Relief Extra Strength
    49035-278Pain Relief Extra StrengthPain Relief Extra Strength
    49738-780Pain Relief Extra StrengthPain Relief Extra Strength
    49738-519Pain Relief Extra StrengthPain Relief Extra Strength
    50844-951Pain Relief Extra StrengthPain Relief Extra Strength
    50804-826Pain Relief Extra StrengthPain Relief Extra Strength
    51013-107Pain Relief Extra StrengthPain Relief Extra Strength
    52904-446Pain Relief Extra StrengthPain Relief Extra Strength
    53345-019Pain Relief Extra StrengthPain Relief Extra Strength
    55316-457Pain Relief Extra StrengthPain Relief Extra Strength
    55316-016Pain Relief Extra StrengthPain Relief Extra Strength
    55319-494Pain Relief Extra StrengthPain Relief Extra Strength
    55910-812Pain Relief Extra StrengthPain Relief Extra Strength
    56062-484pain relief extra strengthpain relief extra strength
    55910-519Pain Relief Extra StrengthPain Relief Extra Strength
    59779-975pain relief extra strengthpain relief extra strength
    59726-494Pain Relief Extra StrengthPain Relief Extra Strength
    59779-751Pain Relief Extra StrengthPain Relief Extra Strength
    59779-872Pain Relief Extra StrengthPain Relief Extra Strength
    59779-757Pain Relief Extra StrengthPain Relief Extra Strength
    59779-519Pain Relief Extra StrengthPain Relief Extra Strength
    59779-484pain relief extra strengthpain relief extra strength
    63868-088Pain Relief Extra StrengthPain Relief Extra Strength
    63868-507Pain Relief Extra StrengthPain Relief Extra Strength
    63868-083Pain Relief Extra StrengthPain Relief Extra Strength
    63941-519Pain Relief Extra StrengthPain Relief Extra Strength
    63868-503Pain Relief Extra StrengthPain Relief Extra Strength
    63868-084Pain Relief Extra StrengthPain Relief Extra Strength
    0121-0657AcetaminophenAcetaminophen
    0113-7000Basic Care acetaminophenAcetaminophen
    0113-7484basic care acetaminophenAcetaminophen
    0113-7544Basic Care AcetaminophenAcetaminophen

    Trademark Results [Pain Relief]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    PAIN RELIEF
    PAIN RELIEF
    97238381 not registered Live/Pending
    Liu, Caiqing
    2022-01-25

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