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  4. NDC Product Code: 69670-218 Alka-seltzer Original

NDC 69670-218 Alka-seltzer Original

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 69670-218?
  5. Alka-seltzer Original Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
69670-218
Proprietary Name:
Alka-seltzer Original
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Impulsora Sahuayo, S.a. De C.v
Labeler Code:
69670
Product Label ID:
c83bec95-c837-656f-e053-2a95a90a41bb
Start Marketing Date: [9]
07-28-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Shape:
ROUND (C48348)
Size(s):
14 MM
Imprint(s):
ALKA;SELTZER
Score:
1

Code Structure Chart

Product Details

What is NDC 69670-218?

The NDC code 69670-218 is assigned by the FDA to the product Alka-seltzer Original which is product labeled by Impulsora Sahuayo, S.a. De C.v. The product's dosage form is . The product is distributed in a single package with assigned NDC code 69670-218-14 150 box in 1 box / 6 pouch in 1 box (69670-218-13) / 2 tablet in 1 pouch (69670-218-12). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Alka-seltzer Original?

● fully dissolve 2 tablets in 4 ounces of water before takingadults and children12 years and over2 tablets every 4hours, or asdirected by a doctordo not exceed 8tablets in 24 hoursadults 60 yearsand over2 tablets every 4hours, or asdirected by a doctordo not exceed 4tablets in 24 hourschildren under12 yearsconsult a doctor

Which are Alka-seltzer Original UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Alka-seltzer Original Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".