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  5. NDC Package Code: 81803-030-02 Safe Opa

NDC Package 81803-030-02 Safe Opa

O-phthalaldehyde Liquid Topical - 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:
81803-030-02
Package Description:
1 BOTTLE in 1 CARTON / 4000 mL in 1 BOTTLE (81803-030-01)
Product Code:
81803-030
Proprietary Name:
Safe Opa
Non-Proprietary Name:
O-phthalaldehyde
Substance Name:
O-phthalaldehyde
Usage Information:
■Rinse thoroughly for more than 5 minutes. Rinse for more than 15 seconds with sterile purified water flowing out after soaking.■After the disinfection of the medical instrument is completed, confirm the persistence.■Excess water may be used depending on the purpose of use.
11-Digit NDC Billing Format:
81803003002
Product Type:
Human Otc Drug
Labeler Name:
Valley Inc.
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
    • Active Ingredient(s):
  • O-PHTHALALDEHYDE 22 g/4000mL
    • 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:
    05-01-2022
    Listing Expiration Date:
    12-31-2024
    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 81803-030-02?

    The NDC Packaged Code 81803-030-02 is assigned to a package of 1 bottle in 1 carton / 4000 ml in 1 bottle (81803-030-01) of Safe Opa, a human over the counter drug labeled by Valley Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 81803-030 included in the NDC Directory?

    Yes, Safe Opa with product code 81803-030 is active and included in the NDC Directory. The product was first marketed by Valley Inc. on May 01, 2022 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 81803-030-02?

    The 11-digit format is 81803003002. 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
    5-3-281803-030-025-4-281803-0030-02