1. Home
  2. Labeler Index
  3. Elysium Consumer Healthcare Llc
  4. 87033-2000
  5. NDC Package Code: 87033-2000-1 Purpose Dual Treatment Spf 10

NDC Package 87033-2000-1 Purpose Dual Treatment Spf 10

Octinoxate 7.5%,Octisalate 5%,Oxybenzone 3% 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:
87033-2000-1
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 113 g in 1 BOTTLE, PLASTIC
Product Code:
87033-2000
Proprietary Name:
Purpose Dual Treatment Spf 10
Non-Proprietary Name:
Octinoxate 7.5%, Octisalate 5%, Oxybenzone 3%
Substance Name:
Octinoxate; Octisalate; Oxybenzone
Usage Information:
Apply generously and evenly 15 minutes before sun exposureapply to all skin exposed to the sunuse a water reistant sunscreen if swimming or sweatingreapply at least every 2 hourschildren un 6 months of age: Ask a doctor
11-Digit NDC Billing Format:
87033200001
Product Type:
Human Otc Drug
Labeler Name:
Elysium Consumer Healthcare 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.
Active Ingredient(s):
Sample Package:
No
FDA Application Number:
M020
Marketing Category:
OTC MONOGRAPH DRUG -
Start Marketing Date:
08-29-2025
Listing Expiration Date:
12-31-2026
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 87033-2000-1?

The NDC Packaged Code 87033-2000-1 is assigned to a package of 1 bottle, plastic in 1 carton / 113 g in 1 bottle, plastic of Purpose Dual Treatment Spf 10, a human over the counter drug labeled by Elysium Consumer Healthcare Llc. The product's dosage form is lotion and is administered via topical form.

Is NDC 87033-2000 included in the NDC Directory?

Yes, Purpose Dual Treatment Spf 10 with product code 87033-2000 is active and included in the NDC Directory. The product was first marketed by Elysium Consumer Healthcare Llc on August 29, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 87033-2000-1?

The 11-digit format is 87033200001. 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 5-4-1 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
5-4-187033-2000-15-4-287033-2000-01