NDC 51596-008

Ache and Pain Relief to Go

Aspirin And Caffeine

Ache and Pain Relief to Go is a Oral Powder in the Human Otc Drug category. It is labeled and distributed by Breakthrough Products Inc.. The primary component is Aspirin; Caffeine.

• Product ID: 51596-008_11bf8091-bb9d-48a5-ba03-a6886a0da329
• NDC: 51596-008
• Product Type: Human Otc Drug
• Proprietary Name: Ache and Pain Relief to Go
• Generic Name: Aspirin And Caffeine
• Dosage Form: Powder
• Route of Administration: ORAL
• Marketing Start Date: 2012-10-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Breakthrough Products Inc.
• Substance Name: ASPIRIN; CAFFEINE
• Active Ingredient Strength: 650 mg/1; mg/1
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 51596-008-01

1 POWDER in 1 POUCH (51596-008-01)

• Marketing Start Date: 2012-10-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 51596-008-12 [51596000812]

Ache and Pain Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

NDC 51596-008-10 [51596000810]

Ache and Pain Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2014-10-16
• Inactivation Date: 2020-01-31

NDC 51596-008-01 [51596000801]

Ache and Pain Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

NDC 51596-008-05 [51596000805]

Ache and Pain Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

NDC 51596-008-24 [51596000824]

Ache and Pain Relief to Go POWDER

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2012-10-01
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
ASPIRIN	650 mg/1

OpenFDA Data

• SPL SET ID: bc31d987-e59d-4386-b421-199ae11d4024
• Manufacturer:
  • Breakthrough Products Inc.
• UNII:
  • R16CO5Y76E
  • 3G6A5W338E
• RxNorm Concept Unique ID - RxCUI:
  • 1312718
• 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 "Ache and Pain Relief to Go" or generic name "Aspirin And Caffeine"

NDC	Brand Name	Generic Name
51596-008	Ache and Pain Relief to Go	aspirin and caffeine
63736-211	Anacin	Aspirin and Caffeine
0280-2635	Bayer	Aspirin and Caffeine
0280-0064	Bayer Headache	Aspirin and caffeine
63029-201	BC	Aspirin and Caffeine
63029-992	BC	Aspirin and Caffeine
63029-202	BC Arthritis	Aspirin and Caffeine
63029-990	BC Arthritis	Aspirin and Caffeine
63029-200	BC Cherry	Aspirin and Caffeine
66715-9815	BC Cherry	Aspirin and Caffeine
63941-402	Best Choice Pain Relief Powder	Aspirin and Caffeine
55910-695	Dollar General Headache Powders	Aspirin and Caffeine
63029-665	GOODYS	aspirin and caffeine
51596-007	Headache Relief to Go	aspirin and caffeine
63868-661	Quality Choice Pain Relief Powder	Aspirin and Caffeine
10956-501	Reese Headache Powders	Aspirin and Caffeine
63029-501	Stanback	Aspirin and Caffeine
0363-8712	Walgreens Headache Powders	Aspirin and Caffeine