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  5. NDC Package Code: 70764-201-52 Botanical Soothing Spf-30

NDC Package 70764-201-52 Botanical Soothing Spf-30

Octinoxate,Octisalate,Zinc Oxide Cream 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:
70764-201-52
Package Description:
1 BOTTLE in 1 BOX / 74 mL in 1 BOTTLE (70764-201-22)
Product Code:
70764-201
Proprietary Name:
Botanical Soothing Spf-30
Non-Proprietary Name:
Octinoxate, Octisalate, Zinc Oxide
Substance Name:
Octinoxate; Octisalate; Zinc Oxide
Usage Information:
APPLY GENEROUSLY WITH FINGERS TO ENTIRE FACE AND NECK. USE DAILY.
11-Digit NDC Billing Format:
70764020152
Billing Unit:
C112160
Product Type:
Human Otc Drug
Labeler Name:
Control Corrective Skincare Inc
Dosage Form:
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
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):
  • OCTINOXATE 6.9 g/100mL
  • OCTISALATE 3 g/100mL
  • ZINC OXIDE 4 g/100mL
    • Pharmacologic Class(es):
  • Copper Absorption Inhibitor - [EPC] (Established Pharmacologic Class)
  • Decreased Copper Ion Absorption - [PE] (Physiologic Effect)
    • Sample Package:
    No
    FDA Application Number:
    part352
    Marketing Category:
    OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
    Start Marketing Date:
    06-08-2016
    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 70764-201-52?

    The NDC Packaged Code 70764-201-52 is assigned to a package of 1 bottle in 1 box / 74 ml in 1 bottle (70764-201-22) of Botanical Soothing Spf-30, a human over the counter drug labeled by Control Corrective Skincare Inc. The product's dosage form is cream and is administered via topical form.

    Is NDC 70764-201 included in the NDC Directory?

    Yes, Botanical Soothing Spf-30 with product code 70764-201 is active and included in the NDC Directory. The product was first marketed by Control Corrective Skincare Inc on June 08, 2016 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 NDC billing unit for package 70764-201-52?

    The contents of this package are billed C112160

    What is the 11-digit format for NDC 70764-201-52?

    The 11-digit format is 70764020152. 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
    5-3-270764-201-525-4-270764-0201-52