NDC Package 65197-202-14 Emetrol Children Mixed Berry

Phosphorated Carbohydrate Solution Oral - View Billable Units, 11-Digit Format, RxNorm

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:
65197-202-14
Package Description:
1 BOTTLE in 1 CARTON / 118 mL in 1 BOTTLE
Product Code:
Proprietary Name:
Emetrol Children Mixed Berry
Non-Proprietary Name:
Phosphorated Carbohydrate
Substance Name:
Dextrose; Fructose; Phosphoric Acid
Usage Information:
For maximum effectiveness never dilute or drink fluids of any kind immediately before or after taking this productrepeat dose every 15 minutes or until distress subsidesChild should not take more than 5 doses in 1 hour without consulting a doctormeasure only with dosing cup provided. Dosing cup to be used with Emetrol only. Do not use with other products. mL= milliliterchildren under 2 years - Do not useĀ children 2 to under 12 years of age - 5 mL or 10mLchildren 12 years of age and over - 15 mL or 30 mL
11-Digit NDC Billing Format:
65197020214
NDC to RxNorm Crosswalk:
  • RxCUI: 318146 - dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG in 5 mL Oral Solution
  • RxCUI: 318146 - fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution
  • RxCUI: 318146 - dextrose 1.87 GM / fructose 1.87 GM / phosphoric acid 21.5 MG per 5 ML Oral Solution
  • RxCUI: 809602 - Emetrol 1.87 GM / 1.87 GM / 21.5 MG in 5 mL Oral Solution
  • RxCUI: 809602 - fructose 374 MG/ML / glucose 374 MG/ML / phosphoric acid 4.3 MG/ML Oral Solution [Emetrol]
Product Type:
Human Otc Drug
Labeler Name:
Wellspring Pharmaceutical Corporation
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Sample Package:
No
Marketing Category:
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date:
06-01-2023
Listing Expiration Date:
12-31-2026
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.

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Frequently Asked Questions

What is NDC 65197-202-14?

The NDC Packaged Code 65197-202-14 is assigned to a package of 1 bottle in 1 carton / 118 ml in 1 bottle of Emetrol Children Mixed Berry, a human over the counter drug labeled by Wellspring Pharmaceutical Corporation. The product's dosage form is solution and is administered via oral form.

Is NDC 65197-202 included in the NDC Directory?

Yes, Emetrol Children Mixed Berry with product code 65197-202 is active and included in the NDC Directory. The product was first marketed by Wellspring Pharmaceutical Corporation on June 01, 2023 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 65197-202-14?

The 11-digit format is 65197020214. 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
5-3-265197-202-145-4-265197-0202-14