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  5. NDC Package Code: 10202-664-69 Antispetic

NDC Package 10202-664-69 Antispetic

Eucalyptol,Menthol,Methyl Salicylate,Thymol Mouthwash Oral - 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:
10202-664-69
Package Description:
250 mL in 1 BOTTLE, PLASTIC
Product Code:
10202-664
Proprietary Name:
Antispetic
Non-Proprietary Name:
Eucalyptol, Menthol, Methyl Salicylate, Thymol
Substance Name:
Eucalyptol; Menthol; Methyl Salicylate; Thymol
Usage Information:
Do not swallownot intended to replace brushing or flossingadults and children 12 years of age and older - vigorously swish 20 mL (2/3 FL OZ or 4 teaspoonfuls) between teeth for 30 seconds then spit outchildren under 12 years of age - consult a dentist or doctor
11-Digit NDC Billing Format:
10202066469
NDC to RxNorm Crosswalk:
  • RxCUI: 1043619 - eucalyptol 0.092 % / menthol 0.042 % / methyl salicylate 0.06 % / thymol 0.064 % Mouthwash
  • RxCUI: 1043619 - eucalyptol 0.92 MG/ML / menthol 0.42 MG/ML / methyl salicylate 0.6 MG/ML / thymol 0.64 MG/ML Mouthwash
    • Product Type:
    Human Otc Drug
    Labeler Name:
    7-eleven
    Dosage Form:
    Mouthwash - An aqueous solution which is most often used for its deodorant, refreshing, or antiseptic effect.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • EUCALYPTOL .92 mg/mL
  • MENTHOL .42 mg/mL
  • METHYL SALICYLATE .6 mg/mL
  • THYMOL .64 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    04-13-2016
    Listing Expiration 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.

    Frequently Asked Questions

    What is NDC 10202-664-69?

    The NDC Packaged Code 10202-664-69 is assigned to a package of 250 ml in 1 bottle, plastic of Antispetic, a human over the counter drug labeled by 7-eleven. The product's dosage form is mouthwash and is administered via oral form.

    Is NDC 10202-664 included in the NDC Directory?

    Yes, Antispetic with product code 10202-664 is active and included in the NDC Directory. The product was first marketed by 7-eleven on April 13, 2016 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 10202-664-69?

    The 11-digit format is 10202066469. 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
    5-3-210202-664-695-4-210202-0664-69