NDC 66715-9703

Alka-Seltzer

Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate

Alka-Seltzer is a Oral Tablet, Effervescent in the Human Otc Drug category. It is labeled and distributed by Lil' Drug Store Products, Inc. The primary component is Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate.

• Product ID: 66715-9703_b3362c04-8a9e-4800-e053-2a95a90a983c
• NDC: 66715-9703
• Product Type: Human Otc Drug
• Proprietary Name: Alka-Seltzer
• Generic Name: Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate
• Dosage Form: Tablet, Effervescent
• Route of Administration: ORAL
• Marketing Start Date: 2000-01-01
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Labeler Name: Lil' Drug Store Products, Inc
• 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: 2021-12-31

Packaging

NDC 66715-9703-1

1 POUCH in 1 CARTON (66715-9703-1) > 2 TABLET, EFFERVESCENT in 1 POUCH

• Marketing Start Date: 2000-01-01
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 66715-9703-0 [66715970300]

Alka-Seltzer TABLET, EFFERVESCENT

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2000-01-01
• Marketing End Date: 2018-12-31

NDC 66715-9703-1 [66715970301]

Alka-Seltzer TABLET, EFFERVESCENT

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2000-01-01

NDC 66715-9703-2 [66715970302]

Alka-Seltzer TABLET, EFFERVESCENT

• Marketing Category: OTC MONOGRAPH NOT FINAL
• Application Number: part343
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2000-01-01

Drug Details

Active Ingredients

Ingredient	Strength
ANHYDROUS CITRIC ACID	1000 mg/1

OpenFDA Data

• SPL SET ID: fbfa46b6-1773-4053-b323-66f4321d6472
• Manufacturer:
  • Lil' Drug Store Products, Inc
• UNII:
  • XF417D3PSL
  • 8MDF5V39QO
  • R16CO5Y76E
• RxNorm Concept Unique ID - RxCUI:
  • 1536680
  • 1536675
• 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" or generic name "Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate"

NDC	Brand Name	Generic Name
53666-218	Alka-Seltzer	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE
66715-5106	Alka-Seltzer	Aspirin, Citric Acid, Sodium Bicarbonate effervescent tablet
66715-9703	Alka-Seltzer	Anhydrous Citric Acid, Aspirin, and Sodium Bicarbonate
69670-218	Alka-Seltzer	ASPIRIN, CITRIC ACID, SODIUM BICARBONATE
50269-307	Alka Seltzer Originial 1s Blister Pack	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
0280-0084	Alka-Seltzer Hangover Relief	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
0280-4000	Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
65662-005	Alka-Seltzer Original	anhydrous citric acid, aspirin, and sodium bicarbonate
70262-304	Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE
70264-014	Alka-Seltzer Original	ANHYDROUS CITRIC ACID, ASPIRIN, and SODIUM BICARBONATE