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  5. NDC Package Code: 84345-086-01 Carekon Anti-cavity Fluoride

NDC Package 84345-086-01 Carekon Anti-cavity Fluoride

Sodium Monofluorophosphate Paste Dental - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
84345-086-01
Package Description:
1 TUBE in 1 BOX / 100 g in 1 TUBE
Product Code:
84345-086
Proprietary Name:
Carekon Anti-cavity Fluoride
Non-Proprietary Name:
Sodium Monofluorophosphate
Substance Name:
Sodium Monofluorophosphate
Usage Information:
Adults and children 2 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor.Instruct children under 6 years of age in good brushing and rinsing habits (to minimize swallowing). Supervise children as necessary until capable of using without supervision.Children under 2 years of age: Consult a dentist or doctor.
11-Digit NDC Billing Format:
84345008601
Product Type:
Human Otc Drug
Labeler Name:
Hunan Yinhuatang Pharmaceutical Technology Co., Ltd.
Dosage Form:
Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route(s):
Dental - Administration to a tooth or teeth.
Active Ingredient(s):
SODIUM MONOFLUOROPHOSPHATE .76 g/100g
Sample Package:
No
FDA Application Number:
M021
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-06-2025
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.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 84345-086-01?

The NDC Packaged Code 84345-086-01 is assigned to a package of 1 tube in 1 box / 100 g in 1 tube of Carekon Anti-cavity Fluoride, a human over the counter drug labeled by Hunan Yinhuatang Pharmaceutical Technology Co., Ltd.. The product's dosage form is paste and is administered via dental form.

Is NDC 84345-086 included in the NDC Directory?

Yes, Carekon Anti-cavity Fluoride with product code 84345-086 is active and included in the NDC Directory. The product was first marketed by Hunan Yinhuatang Pharmaceutical Technology Co., Ltd. on August 06, 2025 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 84345-086-01?

The 11-digit format is 84345008601. 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
5-3-284345-086-015-4-284345-0086-01