NDC Package 62032-116-36 Nu-derm Sunfader Skin Lightener With Sunscreen (spf 15) Paba Free

Hydroquinone,Octinoxate,And Oxybenzone Lotion Topical - View Billable Units, 11-Digit Format, RxNorm

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:
62032-116-36
Package Description:
57 g in 1 BOTTLE, PLASTIC
Product Code:
Proprietary Name:
Nu-derm Sunfader Skin Lightener With Sunscreen (spf 15) Paba Free
Non-Proprietary Name:
Hydroquinone, Octinoxate, And Oxybenzone
Substance Name:
Hydroquinone; Octinoxate; Oxybenzone
Usage Information:
For the gradual bleaching of hyperpigmented skin conditions such as chloasma, melasma, freckles, senile lentigines, and other unwanted areas of melanin hyperpigmentation.
11-Digit NDC Billing Format:
62032011636
NDC to RxNorm Crosswalk:
  • RxCUI: 1235391 - hydroquinone 4 % Topical Lotion
  • RxCUI: 1235391 - hydroquinone 40 MG/ML Topical Lotion
  • RxCUI: 1235391 - hydroquinone 4 % Topical Emulsion
  • RxCUI: 197795 - hydroquinone 4 % Topical Cream
  • RxCUI: 197795 - hydroquinone 40 MG/ML Topical Cream
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Obagi Cosmeceuticals Llc
    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.
  • 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:
    01-01-1984
    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 62032-116-36?

    The NDC Packaged Code 62032-116-36 is assigned to a package of 57 g in 1 bottle, plastic of Nu-derm Sunfader Skin Lightener With Sunscreen (spf 15) Paba Free, a human prescription drug labeled by Obagi Cosmeceuticals Llc. The product's dosage form is lotion and is administered via topical form.

    Is NDC 62032-116 included in the NDC Directory?

    Yes, Nu-derm Sunfader Skin Lightener With Sunscreen (spf 15) Paba Free with product code 62032-116 is active and included in the NDC Directory. The product was first marketed by Obagi Cosmeceuticals Llc on January 01, 1984 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 62032-116-36?

    The 11-digit format is 62032011636. 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
    5-3-262032-116-365-4-262032-0116-36