NDC 70518-0852

Pain Reliever Plus

Acetaminophen, Aspirin And Caffeine

Pain Reliever Plus is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Remedyrepack Inc.. The primary component is Acetaminophen; Aspirin; Caffeine.

• Product ID: 70518-0852_6546c8e3-2108-ae81-e053-2a91aa0a1e51
• NDC: 70518-0852
• Product Type: Human Otc Drug
• Proprietary Name: Pain Reliever Plus
• Generic Name: Acetaminophen, Aspirin And Caffeine
• Dosage Form: Tablet, Film Coated
• Route of Administration: ORAL
• Marketing Start Date: 2017-11-16
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: REMEDYREPACK INC.
• Substance Name: ACETAMINOPHEN; ASPIRIN; CAFFEINE
• Active Ingredient Strength: 250 mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 70518-0852-1

24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0852-1)

• Marketing Start Date: 2018-02-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 70518-0852-2 [70518085202]

Pain Reliever Plus TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2020-05-12

NDC 70518-0852-1 [70518085201]

Pain Reliever Plus TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2018-02-15

NDC 70518-0852-0 [70518085200]

Pain Reliever Plus TABLET, FILM COATED

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2017-11-16
• Marketing End Date: 2020-05-14

Drug Details

Active Ingredients

Ingredient	Strength
ACETAMINOPHEN	250 mg/1

OpenFDA Data

• SPL SET ID: f01fc355-a746-40b8-bc4a-c2e24cfeb9ec
• Manufacturer:
  • REMEDYREPACK INC.
• UNII:
  • 362O9ITL9D
  • R16CO5Y76E
  • 3G6A5W338E
• RxNorm Concept Unique ID - RxCUI:
  • 308297
• Pharm Class PE:
  • Decreased Prostaglandin Production [PE]
  • Decreased Platelet Aggregation [PE]
• PHarm Class EPC:
  • Nonsteroidal Anti-inflammatory Drug [EPC]
  • Platelet Aggregation Inhibitor [EPC]
• NUI Code:
  • N0000008832
  • N0000008836
  • N0000175721
  • N0000000160
  • N0000175578
  • N0000175722

NDC Crossover Matching brand name "Pain Reliever Plus" or generic name "Acetaminophen, Aspirin And Caffeine"

NDC	Brand Name	Generic Name
0904-5135	Pain Reliever Plus	Acetaminophen, Aspirin and caffeine
68151-4672	Pain Reliever Plus	Pain Reliever Plus
69189-5135	Pain Reliever Plus	Pain Reliever Plus
70518-0852	Pain Reliever Plus	Pain Reliever Plus
58118-5135	Pain Reliever Plus	Pain Reliever Plus
15338-703	EXTRA PAIN RELIEF	ACETAMINOPHEN, ASPIRIN AND CAFFEINE
49483-370	EXTRA PAIN RELIEF	ACETAMINOPHEN, ASPIRIN AND CAFFEINE
50268-053	EXTRA PAIN RELIEF	ACETAMINOPHEN, ASPIRIN AND CAFFEINE
49781-065	Extra Strength Headache Relief	Acetaminophen, Aspirin and caffeine
0363-0443	Headache Relief	Acetaminophen, Aspirin and Caffeine
33992-0159	Headache Relief	Acetaminophen, Aspirin and caffeine
36800-283	Headache Relief	ACETAMINOPHEN, ASPIRIN and CAFFEINE
41226-370	HEADACHE RELIEF	ACETAMINOPHEN, ASPIRIN AND CAFFEINE
41520-883	Headache Relief	ACETAMINOPHEN, ASPIRIN and CAFFEINE
42507-184	Headache relief	Acetaminophen, Aspirin and Caffeine
46122-104	Headache relief	Acetaminophen, Aspirin and Caffeine
49035-334	Headache Relief	Acetaminophen, Aspirin and Caffeine
49035-433	Headache Relief	Acetaminophen, Aspirin and Caffeine
49738-183	Headache Relief	ACETAMINOPHEN, ASPIRIN and CAFFEINE
50804-184	Headache relief	Acetaminophen, Aspirin and Caffeine
50804-283	Headache Relief	ACETAMINOPHEN, ASPIRIN and CAFFEINE
50844-159	Headache Relief	Acetaminophen, Aspirin and Caffeine
15127-857	Pain Relief	Acetaminophen, Aspirin and caffeine
11822-1590	Pain Reliever	Acetaminophen, Aspirin and caffeine