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  5. NDC Package Code: 29485-7535-3 Alka-seltzer Original

NDC Package 29485-7535-3 Alka-seltzer Original

Anhydrous Citric Acid,Aspirin,And Sodium Bicarbonate Tablet,Effervescent Tablet, - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
29485-7535-3
Package Description:
30 PACKET in 1 BOX / 2 TABLET, EFFERVESCENT in 1 PACKET
Product Code:
29485-7535
Proprietary Name:
Alka-seltzer Original
Non-Proprietary Name:
Anhydrous Citric Acid, Aspirin, And Sodium Bicarbonate Tablet, Effervescent
Substance Name:
Anhydrous Citric Acid; Aspirin; Sodium Bicarbonate
Usage Information:
• fully dissolve 2 tablets in 4 ounces of water before takingadults and children 12 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 8 tablets in 24 hoursadults 60 years and over2 tablets every 4 hours, or as directed by a doctordo not exceed 4 tablets in 24 hourschildren under 12 yearsconsult a doctor
11-Digit NDC Billing Format:
29485753503
NDC to RxNorm Crosswalk:
  • RxCUI: 1536675 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536675 - ASA 325 MG / Citric Acid 1000 MG / NaHCO3 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536680 - Alka-Seltzer 325 MG / 1000 MG / 1916 MG Effervescent Oral Tablet
  • RxCUI: 1536680 - aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG Effervescent Oral Tablet [Alka-Seltzer]
  • RxCUI: 1536680 - Alka-Seltzer (aspirin 325 MG / citric acid 1000 MG / sodium bicarbonate 1916 MG) Effervescent Oral Tablet
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Lil' Drug Store Products, Inc.
    Dosage Form:
    Tablet, Effervescent - A solid dosage form containing mixtures of acids (e.g., citric acid, tartaric acid) and sodium bicarbonate, which release carbon dioxide when dissolved in water; it is intended to be dissolved or dispersed in water before administration.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ANHYDROUS CITRIC ACID 1000 mg/1
  • ASPIRIN 325 mg/1
  • SODIUM BICARBONATE 1916 mg/1
    • Pharmacologic Class(es):
  • Acidifying Activity - [MoA] (Mechanism of Action)
  • Alkalinizing Activity - [MoA] (Mechanism of Action)
  • Anti-Inflammatory Agents, Non-Steroidal - [CS]
  • Anti-coagulant - [EPC] (Established Pharmacologic Class)
  • Calcium Chelating Activity - [MoA] (Mechanism of Action)
  • Calculi Dissolution Agent - [EPC] (Established Pharmacologic Class)
  • Cyclooxygenase Inhibitors - [MoA] (Mechanism of Action)
  • Decreased Coagulation Factor Activity - [PE] (Physiologic Effect)
  • Decreased Platelet Aggregation - [PE] (Physiologic Effect)
  • Decreased Prostaglandin Production - [PE] (Physiologic Effect)
  • Nonsteroidal Anti-inflammatory Drug - [EPC] (Established Pharmacologic Class)
  • Platelet Aggregation Inhibitor - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    M013
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-17-2016
    End Marketing Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    29485-7535-225 PACKET in 1 BOX / 2 TABLET, EFFERVESCENT in 1 PACKET

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 29485-7535-3?

    The NDC Packaged Code 29485-7535-3 is assigned to a package of 30 packet in 1 box / 2 tablet, effervescent in 1 packet of Alka-seltzer Original, a human over the counter drug labeled by Lil' Drug Store Products, Inc.. The product's dosage form is tablet, effervescent and is administered via oral form.

    Is NDC 29485-7535 included in the NDC Directory?

    Yes, Alka-seltzer Original with product code 29485-7535 is active and included in the NDC Directory. The product was first marketed by Lil' Drug Store Products, Inc. on November 17, 2016.

    What is the 11-digit format for NDC 29485-7535-3?

    The 11-digit format is 29485753503. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-129485-7535-35-4-229485-7535-03