NDC 69517-113

Pain Reliever PM

Acetaminophen And Diphenhydramine Hydrochloride

Pain Reliever PM is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Healthlife Of Usa. The primary component is Acetaminophen; Diphenhydramine Hydrochloride.

Product ID69517-113_2424fb86-c3c9-4da7-9684-46dfda9589d1
NDC69517-113
Product TypeHuman Otc Drug
Proprietary NamePain Reliever PM
Generic NameAcetaminophen And Diphenhydramine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-02-09
Marketing CategoryOTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
Application Numberpart343
Labeler NameHealthLife of USA
Substance NameACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
Active Ingredient Strength500 mg/1; mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 69517-113-50

50 POUCH in 1 BOX (69517-113-50) > 2 TABLET in 1 POUCH
Marketing Start Date2016-06-06
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 69517-113-30 [69517011330]

Pain Reliever PM TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-09

NDC 69517-113-25 [69517011325]

Pain Reliever PM TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-06
Inactivation Date2020-01-31

NDC 69517-113-05 [69517011305]

Pain Reliever PM TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-02-09

NDC 69517-113-02 [69517011302]

Pain Reliever PM TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-06
Inactivation Date2020-01-31

NDC 69517-113-50 [69517011350]

Pain Reliever PM TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-06
Inactivation Date2020-01-31

NDC 69517-113-10 [69517011310]

Pain Reliever PM TABLET
Marketing CategoryOTC monograph not final
Application Numberpart343
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-06-06
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
ACETAMINOPHEN500 mg/1

OpenFDA Data

SPL SET ID:7781f5e0-7f32-4e09-afc5-16ede4605ad1
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1092189

    • NDC Crossover Matching brand name "Pain Reliever PM" or generic name "Acetaminophen And Diphenhydramine Hydrochloride"

    NDCBrand NameGeneric Name
    0363-0213Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-0350PAIN RELIEVER PMAcetaminophen, Diphenhydramine HCl
    0363-0556Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-0760Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-0863Pain Reliever PMAcetaminophen, Diphenhydramine HCL
    0363-2035Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    0363-4470Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    15127-033Pain Reliever PMAcetaminophen and Diphenhydramine Hydrochloride
    15127-325Pain Reliever PMAcetaminophen and Diphenhydramine HCl
    36800-466Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    41250-049Pain Reliever PMAcetaminophen, Diphenhydramine HCl
    69517-113Pain Reliever PMPain Reliever PM
    50844-256Pain Reliever PMPain Reliever PM
    54257-278Pain Reliever PMPain Reliever PM
    71679-143Pain Reliever PMPain Reliever PM
    79903-050Pain Reliever PMPain Reliever PM
    0536-1003ACETA-GESICACETAMINOPHEN AND DIPHENHYDRAMINE HYDROCHLORIDE
    30142-193Acetaminophen and Diphenhydramine hydrochlorideAcetaminophen and Diphenhydramine hydrochloride
    37012-771Acetaminophen PMAcetaminophen and Diphenhydramine Hydrochloride
    41163-515Acetaminophen PMAcetaminophen and Diphenhydramine Hydrochloride
    30142-755Extra Strength Acetaminophen PMAcetaminophen and Diphenhydramine Hydrochloride
    21130-095Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    36800-095Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    36800-771Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    37808-795Pain Relief PMAcetaminophen and Diphenhydramine Hydrochloride
    0031-8770Robitussin Honey Severe Cough, Flu Plus Sore Throat Nighttimeacetaminophen and diphenhydramine hydrochloride
    41167-0040Unisom PM Pain Nighttime Sleep Aid and Pain RelieverAcetaminophen and Diphenhydramine Hydrochloride
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