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  5. NDC Package Code: 70712-101-11 Advanced Protection Sunscreen Spf-30

NDC Package 70712-101-11 Advanced Protection Sunscreen Spf-30

Octinoxate,Octisalate,Zinc Oxide Lotion 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:
70712-101-11
Package Description:
100 mL in 1 BOTTLE
Product Code:
70712-101
Proprietary Name:
Advanced Protection Sunscreen Spf-30
Non-Proprietary Name:
Octinoxate, Octisalate, Zinc Oxide
Substance Name:
Octinoxate; Octisalate; Zinc Oxide
Usage Information:
APPLY TO AREAS EXPOSED TO THE SUN. REAPPLY FREQUENTLY, ESPECIALLY AFTER PHYSICAL ACTIVITY OR SWIMMING.sUN ALERT: LIMITING SUN EXPOSURE, WEARING PROTECTIVE CLOTHING, AND USING SUNSCREENS MAY REDUCE THE RISKS OF SKIN AGING, SKIN CANCER, AND OTHER HARMFUL EFFECTS OF THE SUN.
11-Digit NDC Billing Format:
70712010111
Product Type:
Human Otc Drug
Labeler Name:
Botanical Science, Inc.
Dosage Form:
Lotion - An emulsion, liquid1 dosage form. This dosage form is generally for external application to the skin.2
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 7.5 g/100mL
  • OCTISALATE 5 g/100mL
  • ZINC OXIDE 7 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:
    M020
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-07-2017
    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 70712-101-11?

    The NDC Packaged Code 70712-101-11 is assigned to a package of 100 ml in 1 bottle of Advanced Protection Sunscreen Spf-30, a human over the counter drug labeled by Botanical Science, Inc.. The product's dosage form is lotion and is administered via topical form.

    Is NDC 70712-101 included in the NDC Directory?

    Yes, Advanced Protection Sunscreen Spf-30 with product code 70712-101 is active and included in the NDC Directory. The product was first marketed by Botanical Science, Inc. on August 07, 2017 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 70712-101-11?

    The 11-digit format is 70712010111. 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
    5-3-270712-101-115-4-270712-0101-11