NDC 73097-001

Alka Seltzer Original

Anhydrous Citric Acid, Aspirin, Sodium Bicarbonate

Alka Seltzer Original is a Oral Tablet, Effervescent in the Human Otc Drug category. It is labeled and distributed by Savings Distributors Llc. The primary component is Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate.

• Product ID: 73097-001_8d32fcd8-4ae6-1c8d-e053-2a95a90ad4c7
• NDC: 73097-001
• Product Type: Human Otc Drug
• Proprietary Name: Alka Seltzer Original
• Generic Name: Anhydrous Citric Acid, Aspirin, Sodium Bicarbonate
• Dosage Form: Tablet, Effervescent
• Route of Administration: ORAL
• Marketing Start Date: 2019-07-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Savings Distributors LLC
• Substance Name: ANHYDROUS CITRIC ACID; ASPIRIN; SODIUM BICARBONATE
• Active Ingredient Strength: 1000 mg/1; mg/1; mg/1
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 73097-001-02

1 POUCH in 1 CARTON (73097-001-02) > 2 TABLET, EFFERVESCENT in 1 POUCH

• Marketing Start Date: 2019-07-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 73097-001-40 [73097000140]

Alka Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-01

NDC 73097-001-72 [73097000172]

Alka Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-01

NDC 73097-001-02 [73097000102]

Alka Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-01

NDC 73097-001-48 [73097000148]

Alka Seltzer Original TABLET, EFFERVESCENT

• Marketing Category: OTC monograph not final
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2019-07-01

Drug Details

Active Ingredients

Ingredient	Strength
ANHYDROUS CITRIC ACID	1000 mg/1

OpenFDA Data

• SPL SET ID: 8d334678-2fda-75c5-e053-2a95a90ae344
• Manufacturer:
  • Savings Distributors LLC
• UNII:
  • XF417D3PSL
  • 8MDF5V39QO
  • R16CO5Y76E
• 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 "Alka Seltzer Original" or generic name "Anhydrous Citric Acid, Aspirin, Sodium Bicarbonate"

NDC	Brand Name	Generic Name
67751-143	Alka Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, SODIUM BICARBONATE
73097-001	Alka Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, SODIUM BICARBONATE