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  5. NDC Package Code: 70166-059-01 Bismuth Subsalicylate

NDC Package 70166-059-01 Bismuth Subsalicylate

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:
70166-059-01
Package Description:
50 CUP, UNIT-DOSE in 1 CARTON / 15 mL in 1 CUP, UNIT-DOSE
Product Code:
70166-059
Proprietary Name:
Bismuth Subsalicylate
Usage Information:
Shake well before usefor accurate dosing, use dose cupadults and children 12 years and over: 1 dose (2 tbsp or 30 mL) every 1/2 to 1 hour as neededdo not exceed 8 doses (16 tbsp or 240 mL) in 24 hoursuse until diarrhea stops but not more than 2 dayschildren under 12 years: ask a doctordrink plenty of clear fluids to help prevent dehydration caused by diarrhea
11-Digit NDC Billing Format:
70166005901
NDC to RxNorm Crosswalk:
  • RxCUI: 308762 - bismuth subsalicylate 525 MG in 30 mL Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 17.5 MG/ML Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 1.75 % Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 262 MG per 15 ML Oral Suspension
  • RxCUI: 308762 - bismuth subsalicylate 524 MG per 30 ML Oral Suspension
Labeler Name:
Lohxa
Sample Package:
No
FDA Application Number:
part335
Marketing Category:
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date:
05-30-2008
Listing Expiration Date:
12-31-2022
Exclude Flag:
I
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.

Frequently Asked Questions

What is NDC 70166-059-01?

The NDC Packaged Code 70166-059-01 is assigned to a package of 50 cup, unit-dose in 1 carton / 15 ml in 1 cup, unit-dose of Bismuth Subsalicylate, labeled by Lohxa. The product's dosage form is and is administered via form.

Is NDC 70166-059 included in the NDC Directory?

No, Bismuth Subsalicylate with product code 70166-059 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Lohxa on May 30, 2008 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 70166-059-01?

The 11-digit format is 70166005901. 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 5-3-2 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
5-3-270166-059-015-4-270166-0059-01